Structure of PDB 3knx Chain C Binding Site BS02
Receptor Information
>3knx Chain C (length=151) Species:
63746
(Hepatitis C virus (isolate H77)) [
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VEGEVQIVSTATQTFLATCINGVCWTVYHGAGTRTIASPKGPVIQMYTNV
DQDLVGWPAPQGSRSLTPCTCGSSDLYLVTRHADVIPVRRRGDSRGSLLS
PRPISYLKGSSGGPLLCPAGHAVGLFRAAVCTRGVAKAVDFIPVENLETT
M
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
3knx Chain C Residue 902 [
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Receptor-Ligand Complex Structure
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PDB
3knx
Discovery and structure-activity relationship of P1-P3 ketoamide derived macrocyclic inhibitors of hepatitis C virus NS3 protease.
Resolution
2.65 Å
Binding residue
(original residue number in PDB)
C97 C99 C145
Binding residue
(residue number reindexed from 1)
C69 C71 C117
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D81 G137 S139
Catalytic site (residue number reindexed from 1)
H29 D53 G109 S111
Enzyme Commision number
3.4.21.98
: hepacivirin.
3.6.1.15
: nucleoside-triphosphate phosphatase.
3.6.4.13
: RNA helicase.
Gene Ontology
Molecular Function
GO:0008236
serine-type peptidase activity
Biological Process
GO:0006508
proteolysis
GO:0019087
transformation of host cell by virus
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Molecular Function
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Biological Process
External links
PDB
RCSB:3knx
,
PDBe:3knx
,
PDBj:3knx
PDBsum
3knx
PubMed
19102654
UniProt
Q9ELS8
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