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2A4R

HCV NS3 Protease Domain with a Ketoamide Inhibitor Covalently bound.

Functional Information from GO Data
ChainGOidnamespacecontents
A0006508biological_processproteolysis
A0008236molecular_functionserine-type peptidase activity
A0019087biological_processsymbiont-mediated transformation of host cell
C0006508biological_processproteolysis
C0008236molecular_functionserine-type peptidase activity
C0019087biological_processsymbiont-mediated transformation of host cell
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN A 301
ChainResidue
ACYS97
ATHR98
ACYS99
ACYS145
AHOH405

site_idAC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE BNH A 401
ChainResidue
AILE132
ALYS136
AGLY137
ASER138
ASER139
AARG155
AALA156
AALA157
AVAL158
ACYS159
AHOH470
AGLN41
ATHR42
AHIS57
AARG123

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN C 302
ChainResidue
CCYS97
CCYS99
CCYS145
CHOH304

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsActive site: {"description":"Charge relay system; for serine protease NS3 activity","evidences":[{"source":"PROSITE-ProRule","id":"PRU01166","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"8386278","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"8861917","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues2
DetailsActive site: {"description":"Charge relay system; for serine protease NS3 activity","evidences":[{"source":"PROSITE-ProRule","id":"PRU01166","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"8861917","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues2
DetailsActive site: {"description":"Charge relay system; for serine protease NS3 activity","evidences":[{"source":"PROSITE-ProRule","id":"PRU01166","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"8248148","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"8386278","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"8861917","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU01166","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"21507982","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues22
DetailsRegion: {"description":"NS3-binding","evidences":[{"source":"PubMed","id":"7769699","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"8861917","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1rgq
ChainResidueDetails
AASP81
ASER139
AGLY137
AHIS57

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1rgq
ChainResidueDetails
CASP81
CSER139
CGLY137
CHIS57

site_idMCSA1
Number of Residues
DetailsM-CSA 776
ChainResidueDetails
AHIS57proton shuttle (general acid/base)
AASP81electrostatic stabiliser
AGLY137electrostatic stabiliser
ASER139covalently attached, electrostatic stabiliser

site_idMCSA2
Number of Residues
DetailsM-CSA 776
ChainResidueDetails
CHIS57proton shuttle (general acid/base)
CASP81electrostatic stabiliser
CGLY137electrostatic stabiliser
CSER139covalently attached, electrostatic stabiliser

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PDB entries from 2025-12-24

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