Structure of PDB 1rgq Chain B Binding Site BS02
Receptor Information
>1rgq Chain B (length=186) [
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QMGAPITAYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTATQTFLATC
INGVCWTVYHGAGTRTIASPKGPVIQMYTNVDQDLVGWPAPQGSRSLTPC
TCGSSDLYLVTRHADVIPVRRRGDSRGSLLSPRPISYLKGSSGGPLLCPA
GHAVGLFRAAVCTRGVTKAVDFIPVENLETTMRSGS
Ligand information
>1rgq Chain D (length=17) Species:
3052230
(Hepacivirus hominis) [
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GSVVIVGRIVLSGKPAI
Receptor-Ligand Complex Structure
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PDB
1rgq
Hepatitis C NS3 protease inhibition by peptidyl-alpha-ketoamide inhibitors: kinetic mechanism and structure.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
T7 Y9 Q11
Binding residue
(residue number reindexed from 1)
T7 Y9 Q11
Enzymatic activity
Catalytic site (original residue number in PDB)
H60 D84 G140 S142
Catalytic site (residue number reindexed from 1)
H60 D84 G140 S142
Enzyme Commision number
2.7.7.48
: RNA-directed RNA polymerase.
3.4.21.98
: hepacivirin.
3.4.22.-
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:1rgq
,
PDBe:1rgq
,
PDBj:1rgq
PDBsum
1rgq
PubMed
14984200
UniProt
P27958
|POLG_HCV77 Genome polyprotein
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