Structure of PDB 3eyd Chain A Binding Site BS02
Receptor Information
>3eyd Chain A (length=181) [
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APITAYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTATQTFLATCING
VCWTVYHGAGTRTIASPKGPVIQMYTNVDQDLVGWPAPQGSRSLTPCTCG
SSDLYLVTRHADVIPVRRRGDSRGSLLSPRPISYLKGSSGGPLLCPAGHA
VGLFRAAVCTRGVAKAVDFIPVENLETTMRS
Ligand information
>3eyd Chain D (length=16) Species:
11104
(Hepatitis C virus (isolate 1)) [
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GSVVIVGRIVLSGKPA
Receptor-Ligand Complex Structure
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PDB
3eyd
Potent inhibitors of HCV-NS3 protease derived from boronic acids.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
T4 A5 Y6 A7 Q8
Binding residue
(residue number reindexed from 1)
T4 A5 Y6 A7 Q8
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D81 G137 S139
Catalytic site (residue number reindexed from 1)
H57 D81 G137 S139
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:3eyd
,
PDBe:3eyd
,
PDBj:3eyd
PDBsum
3eyd
PubMed
19022670
UniProt
P26664
|POLG_HCV1 Genome polyprotein
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