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Contact Molecules for Homologous Proteins


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PID QueryLength Homolgous Sequence in PDB UniProt Query TITLE
2932749 515 12 P48551(INAR2_HUMAN) RecName: Full=Interferon alpha/beta receptor 2; Short=IFN-R-2; Short=IFN-alpha binding protein; Short=IFN-alpha/beta receptor 2;AltName: Full=Interferon alpha binding protein;AltName: Full=Type I interferon receptor 2;Flags: Precursor;
QUERYSEQ
MLLSQNAFIFRSLNLVLMVYISLVFGISYDSPDYTDESCTFKISLRNFRSILSWELKNHSIVPTHYTLLYTIMSKPEDLKVVKNCANTTRSFCDLTDEWRSTHEAYVTVLEGFSGNTTLFSCSHNFWLAIDMSFEPPEFEIVGFTNHINV
MVKFPSIVEEELQFDLSLVIEEQSEGIVKKHKPEIKGNMSGNFTYIIDKLIPNTNYCVSVYLEHSDEQAVIKSPLKCTLLPPGQESESAESAKIGGIITVFLIALVLTSTIVTLKWIGYICLRNSLPKVLNFHNFLAWPFPNLPPLEAMD
MVEVIYINRKKKVWDYNYDDESDSDTEAAPRTSGGGYTMHGLTVRPLGQASATSTESQLIDPESEEEPDLPEVDVELPTMPKDSPQQLELLSGPCERRKSPLQDPFPEEDYSSTEGSGGRITFNVDLNSVFLRVLDDEDSDDLEAPLMLS
SHLEEMVDPEDPDNVQSNHLLASGEGTQPTFPSPSSEGLWSEDAPSDQSDTSESDVDLGDGYIMR
[BLAST file for PDB] (plain) (bar) (multiple alignment) [BLAST for UniProt: (plain) (bar) (multiple alignment) (PSSM file) ]

Statistics of sites in view of Disease classification

All LB/B (likely benign or benign)US (uncertain significance)
Number of sites 515 14 1
Buired or ExposedBuried 37.6 (%) [79] 0.0 (%) [0] 0.0 (%) [0]
Exposed 62.4 (%) [131] 100.0 (%) [4] 100.0 (%) [1]
Ave relacc 36.1 % 59.4 % 54.8 %
SD relacc 29.40 % 15.86 % 0.00 %
Contact Molhetero 7.6 (%) [39] 14.3 (%) [2] 0.0 (%) [0]
nucleotide 0.0 (%) [0] 0.0 (%) [0] 0.0 (%) [0]
compound 0.0 (%) [0] 0.0 (%) [0] 0.0 (%) [0]
metal 1.6 (%) [8] 0.0 (%) [0] 0.0 (%) [0]
otherpoly 0.0 (%) [0] 0.0 (%) [0] 0.0 (%) [0]
homo 0.0 (%) [0] 0.0 (%) [0] 0.0 (%) [0]
precipitant 0.0 (%) [0] 0.0 (%) [0] 0.0 (%) [0]
Number of variants 15 14 1
N_Freq(AAvariant)==0 % 57.1 % [8] 100.0 % [1]
N_Freq(AAvariant)>0 % 42.9 % [6] 0.0 % [0]
Ave Freq(AAvariant) 12.6 % 0.0 %
SD Freq(AAvariant) 22.04 % 0.00 %

Site Table for OMIM:LB/B [14 variants]

14 sites 8,10,37,73,196,215,283,295,318,324,346,362,385,450
  [n]:site number of query sequence.  [a]:amino acid of query sequence.  [s]:predicted secondary structure.
  [e]:predicted exposed/buried.  [acc]:predicted relative accesssibility(%).  [pdb]:PDB code of homologous structure.
  [contact_mols]:predicted binding molecules  [observed aa]:Observed amino acids among homologous sequences.  [feature table]:UniProt Feature Table
  [variant]:UniProt Human Variant.
n a s e acc pdb contact_mols observed aa feature table variant
8F----
SVF
SIGNAL DISORDER predicted by DISOPRED SIGNAL F->S:(44.0 %):LB/B - dbSNP:rs2229207
10F----
ILF
SIGNAL DISORDER predicted by DISOPRED SIGNAL F->V:(0.0 %):LB/B - dbSNP:rs1051393
37E e 36.7 2hym_A
E
TOPO_DOM /note="Extracellular" TOPO_DOM /note="Extracellular" E->Q:(0.0 %):LB/B - dbSNP:rs2010033
73MTe 66.7 2hym_A hetero IFNA2_HUMAN Q86UP4_HUMAN IFNW1_HUMAN
M
TOPO_DOM /note="Extracellular" TOPO_DOM /note="Extracellular" M->V:(0.0 %):LB/B - dbSNP:rs1428501
196IEe 54.4 2hym_A
VI
TOPO_DOM /note="Extracellular" TOPO_DOM /note="Extracellular" I->V:(75.0 %):LB/B - dbSNP:rs1786022
215SSe 79.7 2hym_A hetero IFNA2_HUMAN
KSLADEGIPRTVCFHMNQY
TOPO_DOM /note="Extracellular" TOPO_DOM /note="Extracellular" S->G:(2.0 %):LB/B - dbSNP:rs7476057
283H----
YRH
TOPO_DOM /note="Cytoplasmic" TOPO_DOM /note="Cytoplasmic" H->R:(31.0 %):LB/B - dbSNP:rs7635080
295P----
P
TOPO_DOM /note="Cytoplasmic" TOPO_DOM /note="Cytoplasmic" P->L:(0.0 %):LB/B - dbSNP:rs7597449
318Y----
Y
MUTAGEN /note="Y->F: Does not inhibit STAT1, STAT2 and STAT3 activation by IFN. Inhibits STAT1, STAT2 and STAT3 activation by IFN; when associated with F-269; F-306; F- 316; F-337; F-411 and F-512. Inhibits STAT1, STAT2 and STAT3 activation by IFN; when associated with F-269; F-306; F-316; F-411 and F-512. Does not inhibit STAT1, STAT2 and STAT3 activation by IFN; when associated with F-512. Does not inhibit STAT1, STAT2 and STAT3 activation by IFN; when associated with F-269; F-306; F-316 and F-337." ECO:0000269|PubMed:12105218" REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" MUTAGEN /note="Y->F: Does not inhibit STAT1, STAT2 and STAT3 activation by IFN. Inhibits STAT1, STAT2 and STAT3 activation by IFN; when associated with F-269; F-306; F- 316; F-337; F-411 and F-512. Inhibits STAT1, STAT2 and STAT3 activation by IFN; when associated with F-269; F-306; F-316; F-411 and F-512. Does not inhibit STAT1, STAT2 and STAT3 activation by IFN; when associated with F-512. Does not inhibit STAT1, STAT2 and STAT3 activation by IFN; when associated with F-269; F-306; F-316 and F-337." ECO:0000269|PubMed:12105218" REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" Y->C:(0.0 %):LB/B - dbSNP:rs7565715
324S----
SI
REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" DISORDER predicted by DISOPRED REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" S->N:(0.0 %):LB/B - dbSNP:rs2014112
346P----
PAGLSDEFIKNQRTVY
REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" P->S:(2.0 %):LB/B - dbSNP:rs1485198
362P----
PCE
REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" DISORDER predicted by DISOPRED REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" P->S:(0.0 %):LB/B - dbSNP:rs1441207
385P----
PL
REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" REGION /note="Disordered" TOPO_DOM /note="Cytoplasmic" P->L:(22.0 %):LB/B - dbSNP:rs1231284
450S----
SP
TOPO_DOM /note="Cytoplasmic" DISORDER predicted by DISOPRED TOPO_DOM /note="Cytoplasmic" S->L:(0.0 %):LB/B - dbSNP:rs8667333

Site Table for OMIM:US [1 variants]

1 sites 138
  [n]:site number of query sequence.  [a]:amino acid of query sequence.  [s]:predicted secondary structure.
  [e]:predicted exposed/buried.  [acc]:predicted relative accesssibility(%).  [pdb]:PDB code of homologous structure.
  [contact_mols]:predicted binding molecules  [observed aa]:Observed amino acids among homologous sequences.  [feature table]:UniProt Feature Table
  [variant]:UniProt Human Variant.
n a s e acc pdb contact_mols observed aa feature table variant
138EEe 54.8 2hym_A
EK
TOPO_DOM /note="Extracellular" TOPO_DOM /note="Extracellular" E->V:(0.0 %):US -