Contact Molecules for Homologous Proteins | ||||
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PID | QueryLength | Homolgous Sequence in PDB | UniProt Query | TITLE |
3606 | 306 | 500 | YP_009725301.1() | |
QUERYSEQ |
SGFRKMAFPSGKVEGCMVQVTCGTTTLNGLWLDDVVYCPRHVICTSEDMLNPNYEDLLIRKSNHNFLVQAGNVQLRVIGHSMQNCVLKLKVDTANPKTPKYKFVRIQPGQTFSVLACYNGSPSGVYQCAMRPNFTIKGSFLNGSCGSVGF NIDYDCVSFCYMHHMELPTGVHAGTDLEGNFYGPFVDRQTAQAAGTDTTITVNVLAWLYAAVINGDRWFLNRFTTTLNDFNLVAMKYNYEPLTQDHVDILGPLSAQTGIAVLDMCASLKELLQNGMNGRTILGSALLEDEFTPFDVVRQC SGVTFQ |
306 |
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region | name | description |
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1-8 | DISORDER | predicted by DISOPRED |
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|||||||
306 | |||||||
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pdb_id | a1 | identity[%]2 | description | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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A | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
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C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C protein | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C protein | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 Replicase polyprotein 1a | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Main Protease | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 99.7 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 99.7 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 Non-structural protein 7 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | A0A7L9RWV7_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 Replicase polyprotein 1ab | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1A_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1A_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase nsp5 | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 100.0 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | 99.7 | R1AB_SARS2 3C-like proteinase | |||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 99.7 | R1AB_SARS2 Replicase polyprotein 1ab | |||
1.a1:asym_id for the homologue. 2.identity[%]2:sequence identity between the query and the homologue. |
![]() |
|||||||
306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-.. | A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B | N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-.. | A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B | N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-.. | A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | N-[(5-METHYLISOXAZOL-3-YL)CARBONYL]ALANYL-L-VALYL-.. | A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C | inhibitor UAW248[5 aa] | A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | Leupeptin[4 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | Leupeptin[4 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | LEUPEPTIN[4 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | LEUPEPTIN[4 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 3-PYRIDIN-4-YL-2,4-DIHYDRO-INDENO[1,2-.C.]PYRAZOLE.. | A | 100.0 /100.0 |
12 /12 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 3-PYRIDIN-4-YL-2,4-DIHYDRO-INDENO[1,2-.C.]PYRAZOLE.. | A | 100.0 /100.0 |
14 /14 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | 3-PYRIDIN-4-YL-2,4-DIHYDRO-INDENO[1,2-.C.]PYRAZOLE.. | A | 100.0 /100.0 |
14 /14 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | Mpro inhibitor[5 aa] | A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | Mpro inhibitor[5 aa] | A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
![]() |
|||||||
306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
3WL
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
3WL
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
3WL
|
D | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X77
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X77
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
X77
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
X77
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
X77
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
X77
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
X77
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
X77
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
X77
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
X77
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U5G
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
K36
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
K36
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UED
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
UED
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
UED
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
E |
UED
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
E |
UED
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
UED
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NEN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NEN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
NEN
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
NEN
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SV6
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SV6
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SV6
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SV6
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SV6
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SV6
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SV6
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SV6
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SV6
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SV6
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
NNA
|
A | 100.0 /100.0 |
25 /25 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
NNA
|
B | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NNA
|
A | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NNA
|
A | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
V7G
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
V7G
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
P6N
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
P6N
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
P6N
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
P6N
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A82
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A82
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Q5T
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Q5T
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
R6Q
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
R6Q
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
R6Q
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
R6Q
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
R7Q
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
R7Q
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CB1
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CB1
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RMZ
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RMZ
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RMZ
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RMZ
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
RNW
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
RNW
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
RT2
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
RT2
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
RV5
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
RV5
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
RV8
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
RV8
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
S1W
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CLU
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CLU
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
S8H
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
S8H
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
93J
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
93J
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
93J
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
93J
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
QCP
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
QCP
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
S8T
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
S8T
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
S8T
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
S8T
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SQ2
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SQ2
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
SQ5
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
I |
SQ5
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
SQ5
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
SQ5
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
T0W
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
T0W
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
ALD
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
ALD
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ALD
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
ALD
|
B | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ALD
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ALD
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
ALD
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
ALD
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
ALD
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ALD
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JRY
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JRY
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
B1S
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
GQU
|
A | 100.0 /100.0 |
19 /19 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
B |
GQU
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
B |
GQU
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
GQU
|
A | 100.0 /100.0 |
19 /19 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
H6F
|
A | 100.0 /100.0 |
23 /23 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
H6F
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
H6F
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
H6F
|
A | 100.0 /100.0 |
23 /23 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
H6L
|
A | 100.0 /100.0 |
20 /20 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
D |
H6L
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
H6L
|
B | 100.0 /100.0 |
21 /21 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
HER
|
B | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
HUO
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
HUO
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
HYR
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
HYR
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
HYR
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
HYR
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
HYR
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
HYR
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
J7R
|
A | 100.0 /100.0 |
17 /17 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
D |
J7R
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
J7O
|
A | 100.0 /100.0 |
17 /17 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
J7O
|
A | 100.0 /100.0 |
17 /17 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
2RI
|
B | 100.0 /100.0 |
17 /17 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
KFU
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
KG9
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
KG9
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
Q99
|
B | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
OYF
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
OYX
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
OYX
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
OVX
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
P3L
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
P7R
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
PJX
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
OQL
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
OQL
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
PJ6
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
PQ6
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
QCC
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
QD4
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
QD9
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
QD9
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
QDF
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
F |
QE3
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
QE3
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
QER
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
QER
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
QFL
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
QG3
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
QG3
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
QGC
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
QGO
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
QGO
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
QHI
|
B | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
QI7
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
QIT
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
P4R
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
PUU
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
QJL
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
QJR
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
QK3
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
F |
QKB
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
Q0I
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
QKR
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
QM9
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
QML
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
QMX
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
QOO
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
QYI
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
QYN
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
QZC
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
QM3
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
R76
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
R8I
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
R8O
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
R9E
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
R9R
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
RAQ
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
L |
RAQ
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
860
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
860
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
860
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
860
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
860
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
OE6
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RD5
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
RDK
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RFF
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RFR
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RGX
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RI1
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RJ3
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
O |
RJ3
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RJO
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RK6
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
O |
RK6
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
RKC
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RL0
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RL8
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RM3
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RNI
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RPK
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RQO
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RRD
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RRU
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RS6
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RSL
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
RT9
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
RTS
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
RVL
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
O |
RVL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
RVL
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
RVR
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RVR
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
RVR
|
B | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RW9
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
RW9
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RXU
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
Q |
RXU
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
RXU
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
RZU
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
RZU
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
RZU
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
RZU
|
B | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
S0X
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
S1U
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
N |
S1U
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
I |
S1U
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
S1U
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
S1L
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
S |
S1L
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
S3X
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
P |
S3X
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
S4X
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
S5L
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
T |
S5L
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
S6K
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
S7C
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
S7U
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XWH
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
XWZ
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
XWZ
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
Y2C
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
G |
Y2C
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
Y2C
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
Y2C
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
K |
Y25
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
W |
Y25
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
Y1L
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
Y3N
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
NT9
|
B | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
NT9
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
Y0H
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
XZT
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
XZO
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
XZE
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
JAH
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
TG3
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
TG3
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
TG3
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
TG3
|
B | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
TG3
|
C | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
TG3
|
D | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
BTB
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
BTB
|
D | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
BTB
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
0EN
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
0EN
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XF1
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
XF1
|
B | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XF4
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XF4
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XFD
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
XFD
|
B | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
AG7
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
AG7
|
B | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
AG7
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
B |
AG7
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
B |
AG7
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
AG7
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XTJ
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
XTJ
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
XTJ
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XTJ
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XTM
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
D |
XTM
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
XTM
|
B | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XTP
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
XTP
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
XTP
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XTP
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XU4
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XU4
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XV4
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
XV4
|
B | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
C |
Y6J
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
Y6J
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
Y6G
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
D |
Y6G
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
C |
Y6G
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
Y6G
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
YD1
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
YD1
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
YD1
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
YD1
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
YD1
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
YD1
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
YCV
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
YCV
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
YCV
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
YCV
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
YVA
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
D |
YVA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
C |
YVA
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
YVA
|
B | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
YV7
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
D |
YV7
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
H |
YVV
|
C | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
YVV
|
C | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
YWJ
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
H |
YWJ
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
E |
YWJ
|
D | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
YWJ
|
D | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
FN7
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZL7
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZL7
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
ASC
|
B | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
U7W
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
U7W
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
U7W
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
U7W
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
U9H
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
F |
U9H
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
U9H
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
U9H
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
35J
|
A | 100.0 /100.0 |
12 /12 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
35J
|
A | 100.0 /100.0 |
12 /12 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4N0
|
A | 100.0 /100.0 |
14 /14 |
A0A7L9RWV7_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
7IL
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
7IL
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
90I
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
90I
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
90X
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
90X
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
GWS
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
R8H
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
R8H
|
B | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
4IT
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
4IT
|
B | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4IJ
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4IJ
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4I9
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4I9
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
4W8
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5YN
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5YN
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5YJ
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5YJ
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5Z7
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5Z7
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5Z3
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5Z3
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZN
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZN
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZJ
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZJ
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
H69
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
H69
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZW
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZW
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZT
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5ZT
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Z26
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
Z26
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
Z26
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Z26
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
87H
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
87H
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
87H
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
87H
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I70
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I70
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I70
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I70
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8ZI
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8ZI
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
90H
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
90H
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
91I
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
91I
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
91Z
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
91Z
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
99W
|
B | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
99W
|
C | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
99W
|
D | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I1W
|
A | 100.0 /100.0 |
24 /24 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
I1W
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
I1W
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I1W
|
A | 100.0 /100.0 |
24 /24 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I1Z
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I1Z
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NB2
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
NB2
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U88
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
U88
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
U88
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
U88
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
U88
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
U88
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
U88
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
U88
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
O5F
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
O5F
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
5IL
|
A | 100.0 /100.0 |
15 /15 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
3XI
|
A | 100.0 /100.0 |
19 /19 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
3XI
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
B |
3XI
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
3XI
|
A | 100.0 /100.0 |
19 /19 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
G7L
|
A | 100.0 /100.0 |
11 /11 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
G7L
|
A | 100.0 /100.0 |
11 /11 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
G7O
|
B | 100.0 /100.0 |
9 /9 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
BOV
|
A | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
BOV
|
B | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
IFO
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
B |
IFO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
B |
IFO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
IFO
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XNV
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
D |
XNV
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
XNV
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
XNV
|
B | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
V9R
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
V9R
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
V9R
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
V9R
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
MXU
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() |
![]() |
E |
MXU
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
MXU
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
M9X
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
E |
M9X
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
MFL
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
E |
MFL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
C |
MFL
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
MFL
|
B | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
MIJ
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
OW1
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
OW1
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
OW1
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
OW1
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
QH0
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
QH0
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
P5X
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
P5X
|
B | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
P5X
|
C | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
P5X
|
D | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
P6I
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
G |
P6I
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
P6I
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
H |
P6I
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
E |
P6I
|
C | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
P6I
|
C | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
P6I
|
D | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
P6R
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
G |
P6R
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
P6R
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
H |
P6R
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
P6R
|
C | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
F |
P6R
|
D | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
P6R
|
D | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
P7L
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
P7L
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
P7L
|
C | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
P7L
|
D | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
QAO
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
QAO
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
T4V
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
T4V
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SRU
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SRU
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SVL
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
SVL
|
A | 100.0 /100.0 |
10 /10 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
V2M
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X6O
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X6O
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X70
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X70
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X6T
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
X6T
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
X6T
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X6T
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X9Z
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X9Z
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XA8
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
XA8
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Y8O
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
Y8O
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
Y8O
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
Y8O
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
YFK
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
K9U
|
A | 100.0 /100.0 |
17 /17 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
OZB
|
A | 100.0 /100.0 |
22 /22 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
OZB
|
A | 100.0 /100.0 |
22 /22 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
AO0
|
A | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
AO0
|
A | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
VQR
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
VQR
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
VQN
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
VQN
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
B |
VQN
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
VQN
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
83F
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
83N
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
84C
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
83W
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
9M5
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
9M5
|
B | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XI0
|
A | 100.0 /100.0 |
15 /15 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
XI0
|
B | 100.0 /100.0 |
15 /15 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XH9
|
A | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
E |
XH9
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XHW
|
A | 100.0 /100.0 |
16 /16 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
H |
XHW
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
XJ9
|
A | 100.0 /100.0 |
14 /14 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A1H1J
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
B |
A1H1J
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
B |
A1H1J
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A1H1J
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I3R
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I3R
|
A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A1W
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
A1W
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
WGE
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
WGE
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
WZK
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
ZQB
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() |
![]() |
D |
ZQB
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
JVX
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
JVX
|
B | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JJC
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JJC
|
A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JJO
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JJO
|
A | 100.0 /100.0 |
12 /12 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
JK0
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
JK0
|
B | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JWI
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JWI
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JKL
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JKL
|
A | 100.0 /100.0 |
15 /15 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JKL
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JKL
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JWO
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
JWO
|
A | 100.0 /100.0 |
14 /14 |
R1AB_SARS2 Non-structural protein 7 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
W28
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
W28
|
A | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
WOK
|
A | 100.0 /100.0 |
25 /25 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
WOK
|
A | 100.0 /100.0 |
25 /25 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
WTE
|
B | 100.0 /100.0 |
19 /19 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
WTV
|
B | 100.0 /100.0 |
22 /22 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
A1ADS
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X83
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X83
|
A | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X8F
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
X8F
|
A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
A1AD0
|
A | 100.0 /100.0 |
16 /16 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
A1AD0
|
B | 100.0 /100.0 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
T2L
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
T2L
|
A | 100.0 /100.0 |
22 /22 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
21 /21 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /100.0 |
21 /21 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
4WI
|
B | 100.0 /100.0 |
19 /19 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
4WI
|
A | 95.0 /99.7 |
20 /20 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
4WI
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
4WI
|
B | 100.0 /99.7 |
17 /17 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 95.0 /99.7 |
20 /20 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 95.0 /99.7 |
20 /20 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
21 /21 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
21 /21 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 95.2 /99.7 |
21 /21 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 95.2 /99.7 |
21 /21 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
21 /21 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
21 /21 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
21 /21 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
4WI
|
A | 100.0 /99.7 |
20 /20 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
7V2
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
7V2
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
7VI
|
B | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
7VQ
|
A | 100.0 /99.7 |
20 /20 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8GW
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8GW
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I71
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I71
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8H9
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8H9
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I69
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I69
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8I7
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8I7
|
A | 100.0 /99.7 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8T6
|
A | 100.0 /99.7 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8T6
|
A | 100.0 /99.7 |
14 /14 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8UI
|
A | 100.0 /99.7 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
8UI
|
A | 100.0 /99.7 |
17 /17 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I80
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
I80
|
A | 100.0 /99.7 |
19 /19 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
M0C
|
A | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
M0C
|
A | 100.0 /100.0 |
23 /23 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
M0C
|
A | 95.7 /99.7 |
23 /23 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B |
M0C
|
A | 95.7 /99.7 |
23 /23 |
R1AB_SARS2 3C-like proteinase nsp5 |
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D |
O6K
|
B | 94.4 /99.7 |
18 /18 |
R1A_SARS2 3C-like proteinase nsp5 |
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E |
7YY
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
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G |
7YY
|
B | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase nsp5 |
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E |
7YY
|
B | 100.0 /99.7 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
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G |
7YY
|
B | 94.4 /99.7 |
18 /18 |
R1AB_SARS2 Replicase polyprotein 1ab |
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C |
LQZ
|
A | 100.0 /99.7 |
5 /5 |
R1A_SARS2 3C-like proteinase nsp5 |
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C |
LQZ
|
A | 100.0 /99.7 |
5 /5 |
R1A_SARS2 3C-like proteinase nsp5 |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
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|||||||
306 | pdb_id | contact mol | homologue | ||||
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a3 | description | a4 | identity[%]5 | Ncon6 | description | |
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G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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E |
NA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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E |
NA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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S |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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O |
NA
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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C |
NA
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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O |
NA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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H |
NA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
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H |
NA
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
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N |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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O |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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H |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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P |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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I |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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K |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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J |
NA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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U |
NA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
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U |
NA
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
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H |
NA
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
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M |
NA
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
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V |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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L |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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G |
NA
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
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P |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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O |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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K |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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N |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
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M |
NA
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
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G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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G |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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L |
NA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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L |
NA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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C |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
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C |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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E |
NA
|
A | 100.0 /100.0 |
7 /7 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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E |
NA
|
A | 100.0 /100.0 |
7 /7 |
R1A_SARS2 3C-like proteinase |
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C |
NA
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
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C |
NA
|
B | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B |
NA
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
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B |
NA
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
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C |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
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B |
NA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
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B |
NA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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L |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Replicase polyprotein 1ab |
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M |
NA
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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G |
NA
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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L |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C |
NA
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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X |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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K |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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N |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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K |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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E |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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H |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C |
NA
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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H |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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N |
NA
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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O |
NA
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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M |
NA
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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N |
NA
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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M |
NA
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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N |
NA
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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P |
NA
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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H |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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J |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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I |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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J |
NA
|
B | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
T |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Y |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
X |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
P |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
O |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
CL
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
O |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
Q |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /99.7 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /99.7 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /99.7 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /99.7 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
N |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
Y |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
H |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
L |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
P |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
CL
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
CL
|
B | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CL
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
CL
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
CA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
ZN
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
ZN
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
ZN
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
ZN
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
ZN
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
ZN
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 Replicase polyprotein 1a |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
ZN
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 Replicase polyprotein 1a |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
NI
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
D |
NI
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
NI
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
NI
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
NI
|
B | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
NI
|
B | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
J |
NI
|
B | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
BR
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
BR
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
BR
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
BR
|
B | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
BR
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
BR
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
![]() |
|||||||
306 | pdb_id | contact mol | homologue | ||||
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
a3 | description | a4 | identity[%]5 | Ncon6 | description | |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | D | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[304 aa] | A | 100.0 /100.0 |
39 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 Main Protease[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 Main Protease |
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A | R1AB_SARS2 Main Protease[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 Main Protease |
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B | R1AB_SARS2 3C-like proteinase[301 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[307 aa] | B | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C protein[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C protein |
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A | R1AB_SARS2 3C protein[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C protein |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[304 aa] | A | 100.0 /100.0 |
27 /27 |
R1AB_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
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![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase |
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![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase |
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B | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
34 /34 |
R1A_SARS2 3C-like proteinase |
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![]() |
A | R1A_SARS2 3C-like proteinase[304 aa] | B | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
18 /18 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | C | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | C | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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D | R1AB_SARS2 3C-like proteinase[306 aa] | C | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[306 aa] | D | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1A_SARS2 3C-like proteinase[301 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
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![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | R1A_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[297 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[292 aa] | A | 100.0 /100.0 |
32 /32 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[297 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[302 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[297 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[297 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[298 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[296 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[287 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[299 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[302 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | B | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[300 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[303 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[302 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[304 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
33 /33 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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D | R1AB_SARS2 3C-like proteinase[306 aa] | C | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[305 aa] | D | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
47 /47 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
47 /47 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[304 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[302 aa] | C | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[303 aa] | D | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
26 /26 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
26 /26 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
32 /32 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
32 /32 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[303 aa] | B | 100.0 /100.0 |
38 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
48 /48 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
48 /48 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[302 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[304 aa] | A | 100.0 /100.0 |
36 /36 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[300 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[302 aa] | A | 100.0 /100.0 |
36 /36 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
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B | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
41 /41 |
R1A_SARS2 3C-like proteinase |
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B | R1A_SARS2 3C-like proteinase[301 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
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B | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
35 /35 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 Replicase polyprotein 1a[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 Replicase polyprotein 1a |
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A | R1A_SARS2 Replicase polyprotein 1a[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 Replicase polyprotein 1a |
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A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1A_SARS2 3C-like proteinase |
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A | R1AB_SARS2 Replicase polyprotein 1ab[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Replicase polyprotein 1ab |
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A | R1AB_SARS2 Replicase polyprotein 1ab[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Replicase polyprotein 1ab |
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B | R1AB_SARS2 Replicase polyprotein 1ab[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 Replicase polyprotein 1ab |
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A | R1AB_SARS2 Replicase polyprotein 1ab[305 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Replicase polyprotein 1ab |
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B | R1AB_SARS2 Replicase polyprotein 1ab[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 Replicase polyprotein 1ab |
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A | R1AB_SARS2 Replicase polyprotein 1ab[306 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 Replicase polyprotein 1ab |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
43 /43 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[301 aa] | B | 100.0 /100.0 |
32 /32 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
11 /11 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
13 /13 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
43 /43 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
43 /43 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
D | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[303 aa] | C | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
B | R1AB_SARS2 3C-like proteinase[306 aa] | D | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
46 /46 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
46 /46 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
43 /43 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
43 /43 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
43 /43 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[300 aa] | B | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /99.7 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 Replicase polyprotein 1ab[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Replicase polyprotein 1ab |
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A | R1AB_SARS2 Replicase polyprotein 1ab[306 aa] | B | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 Replicase polyprotein 1ab |
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B | R1AB_SARS2 3C-like proteinase nsp5[304 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[303 aa] | B | 100.0 /99.7 |
41 /41 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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D | R1AB_SARS2 3C-like proteinase[306 aa] | C | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[305 aa] | D | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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D | R1AB_SARS2 3C-like proteinase[305 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | C | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | D | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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D | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | C | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | D | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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C | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase |
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D | R1AB_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | C | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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B | R1AB_SARS2 3C-like proteinase[305 aa] | D | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 97.6 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 97.6 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
40 /40 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
40 /40 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /99.7 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 97.6 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 97.6 /99.7 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[303 aa] | B | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[302 aa] | B | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 Replicase polyprotein 1ab[302 aa] | B | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 Replicase polyprotein 1ab |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[302 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 Replicase polyprotein 1ab[299 aa] | A | 100.0 /99.7 |
33 /33 |
R1AB_SARS2 Replicase polyprotein 1ab |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /99.7 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[303 aa] | B | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1A_SARS2 3C-like proteinase[302 aa] | A | 100.0 /100.0 |
32 /32 |
R1A_SARS2 3C-like proteinase |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 97.6 /99.7 |
41 /41 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 97.6 /99.7 |
41 /41 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1AB_SARS2 3C-like proteinase[306 aa] | A | 100.0 /99.7 |
41 /41 |
R1AB_SARS2 3C-like proteinase |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
33 /33 |
R1A_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1A_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
33 /33 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
34 /34 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
B | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | B | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[305 aa] | A | 100.0 /100.0 |
33 /33 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1A_SARS2 3C-like proteinase[306 aa] | B | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[302 aa] | A | 100.0 /100.0 |
31 /31 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[304 aa] | A | 100.0 /100.0 |
35 /35 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B | R1A_SARS2 3C-like proteinase[302 aa] | A | 100.0 /100.0 |
37 /37 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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![]() |
A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
42 /42 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
35 /35 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[304 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | B | 100.0 /100.0 |
41 /41 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | B | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 Non-structural protein 7 |
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![]() |
A | R1AB_SARS2 Non-structural protein 7[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 Non-structural protein 7 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
40 /40 |
R1A_SARS2 3C-like proteinase nsp5 |
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A | R1A_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
38 /38 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | R1AB_SARS2 3C-like proteinase nsp5[301 aa] | B | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
38 /38 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | A | 100.0 /100.0 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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B | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
37 /37 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[305 aa] | B | 100.0 /100.0 |
36 /36 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /100.0 |
40 /40 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
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A | R1AB_SARS2 3C-like proteinase nsp5[306 aa] | A | 100.0 /99.7 |
39 /39 |
R1AB_SARS2 3C-like proteinase nsp5 |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. | |||||||
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|||||||
306 | pdb_id | contact mol | homologue | ||||
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a3 | description | a4 | identity[%]5 | Ncon6 | description | |
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D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
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E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
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G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
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![]() |
Q |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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R |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
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![]() |
F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
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L |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
N |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
H |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
V |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
W |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
X |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
L |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Y |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
V |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
W |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
X |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Y |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
V |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
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D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
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F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
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H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
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![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
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![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
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![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
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![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
V |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
V |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
AA |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
AA |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
BA |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
CA |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
DA |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
U |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
W |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
X |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Y |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Z |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /99.7 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
B |
DMS
|
A | 100.0 /99.7 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /99.7 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /99.7 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /99.7 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /99.7 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /99.7 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /99.7 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /99.7 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /99.7 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /99.7 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() |
![]() |
C |
DMS
|
B | 100.0 /99.7 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /99.7 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /99.7 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /99.7 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /99.7 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /99.7 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /99.7 |
2 /2 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /99.7 |
1 /1 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /99.7 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
B | 100.0 /99.7 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /99.7 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
DMS
|
A | 100.0 /100.0 |
8 /8 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
DMS
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
DMS
|
A | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
DMS
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
DMS
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
DMS
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
DMS
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
DMS
|
B | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
DMS
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
S |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
DMS
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
GOL
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
GOL
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
GOL
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
GOL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
GOL
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
GOL
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C protein |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
GOL
|
B | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
GOL
|
A | 100.0 /99.7 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
GOL
|
A | 100.0 /99.7 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
GOL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
GOL
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
GOL
|
A | 100.0 /100.0 |
9 /9 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
GOL
|
A | 100.0 /100.0 |
9 /9 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
GOL
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
GOL
|
B | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
C |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
C |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
IMD
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
IMD
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
IMD
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IMD
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
IMD
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
IMD
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
EDO
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() |
![]() |
M |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
O |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
P |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
R |
EDO
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
M |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
N |
EDO
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
EDO
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
EDO
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 Replicase polyprotein 1ab |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
K |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
V |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
EDO
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
EDO
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
B | 100.0 /100.0 |
9 /9 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
EDO
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
EDO
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
EDO
|
B | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
EDO
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
EDO
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
EDO
|
B | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
EDO
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
N |
EDO
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
M |
EDO
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
TRS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
TRS
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
SO4
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
SO4
|
A | 100.0 /100.0 |
8 /8 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
SO4
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
SO4
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
SO4
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
SO4
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
D |
SO4
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
SO4
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
D |
SO4
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
SO4
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
ETF
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IPA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IPA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IPA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
IPA
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
IPA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
IPA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
IPA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
IPA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
IPA
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
IPA
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
FMT
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
F |
FMT
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
G |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
K |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
FMT
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
FMT
|
B | 100.0 /100.0 |
5 /5 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
FMT
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
FMT
|
A | 100.0 /100.0 |
4 /4 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
A | 100.0 /100.0 |
2 /2 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
J |
FMT
|
A | 100.0 /100.0 |
1 /1 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
FMT
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
FMT
|
A | 100.0 /100.0 |
6 /6 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
I |
FMT
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
U |
FMT
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() |
![]() |
F |
FMT
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
I |
NO3
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
K |
NO3
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
MLI
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
P |
ACT
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
Q |
ACT
|
B | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
T |
ACT
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
E |
ACT
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
E |
ACT
|
B | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
G |
ACT
|
B | 100.0 /100.0 |
7 /7 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
ACT
|
A | 100.0 /100.0 |
6 /6 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
ACT
|
B | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
S |
MPD
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
J |
MPD
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
L |
MPD
|
B | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
MPD
|
B | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
D |
PGE
|
A | 100.0 /100.0 |
3 /3 |
R1A_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PO4
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PO4
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PO4
|
A | 100.0 /100.0 |
5 /5 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PO4
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() |
![]() |
H |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
I |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
PEG
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
J |
PEG
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
PEG
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
K |
PEG
|
A | 100.0 /100.0 |
1 /1 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
PEG
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
PEG
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
H |
PEG
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() |
![]() |
H |
PEG
|
A | 100.0 /100.0 |
2 /2 |
R1AB_SARS2 3C-like proteinase |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PEG
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PEG
|
A | 100.0 /100.0 |
3 /3 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PEG
|
A | 100.0 /100.0 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PEG
|
A | 100.0 /99.7 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![]() |
C |
PEG
|
A | 100.0 /99.7 |
4 /4 |
R1AB_SARS2 3C-like proteinase nsp5 |
3.a3:asym_id for the contact molecule. 4.a4:asym_id for the template homologue. 5.identity[%]5:sequence identity between the query and the template homologue only for the contact residues. Number after the slash / is sequence identity for all the aligned region. 6.Ncon6:number of aligned contact residues for the query. Number after the slash / is number of contact residues in the template homologue. |