Structure of PDB 5eqs Chain A Binding Site BS02
Receptor Information
>5eqs Chain A (length=192) [
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KKGSVVIVGRINLSGDTAYAQQTRGEEGCQETSQTGRDKNQVEGEVQIVS
TATQTFLATSINGVLWTVYHGAGTRTIASPKGPVTQMYTNVDKDLVGWQA
PQGSRSLTPCTCGSSDLYLVTRHADVIPVRRRGDSTGSLLSPRPLSYLKG
SSGGPLLCPAGHAVGIFRAAVCTRGVAKAVQFIPVESLETTM
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
5eqs Chain A Residue 1202 [
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Receptor-Ligand Complex Structure
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PDB
5eqs
Molecular and Dynamic Mechanism Underlying Drug Resistance in Genotype 3 Hepatitis C NS3/4A Protease.
Resolution
1.839 Å
Binding residue
(original residue number in PDB)
C1097 C1099 C1145
Binding residue
(residue number reindexed from 1)
C110 C112 C158
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H1057 D1081 G1137 S1139
Catalytic site (residue number reindexed from 1)
H70 D94 G150 S152
Enzyme Commision number
3.6.4.13
: RNA helicase.
Gene Ontology
Molecular Function
GO:0008233
peptidase activity
GO:0008236
serine-type peptidase activity
GO:0046872
metal ion binding
Biological Process
GO:0006508
proteolysis
GO:0019062
virion attachment to host cell
GO:0019087
transformation of host cell by virus
GO:0046718
symbiont entry into host cell
Cellular Component
GO:0016020
membrane
GO:0033644
host cell membrane
GO:0044423
virion component
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5eqs
,
PDBe:5eqs
,
PDBj:5eqs
PDBsum
5eqs
PubMed
27512818
UniProt
A0A0B4WYC6
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