Structure of PDB 2fm2 Chain A Binding Site BS02
Receptor Information
>2fm2 Chain A (length=181) [
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APITAYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTATQTFLATCING
VCWTVYHGAGTRTIASPKGPVIQMYTNVDQDLVGWPAPQGSRSLTPCTCG
SSDLYLVTRHADVIPVRRRGDSRGSLLSPRPISYLKGSSGGPLLCPAGHA
VGLFRAAVCTRGVAKAVDFIPVENLETTMRS
Ligand information
>2fm2 Chain D (length=16) Species:
2847144
(hepatitis C virus genotype 1a) [
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GSVVIVGRIVLSGKPA
Receptor-Ligand Complex Structure
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PDB
2fm2
Mutations conferring resistance to SCH6, a novel hepatitis C virus NS3/4A protease inhibitor. Reduced RNA replication fitness and partial rescue by second-site mutations
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
T4 A5 Y6
Binding residue
(residue number reindexed from 1)
T4 A5 Y6
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
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:2fm2
,
PDBe:2fm2
,
PDBj:2fm2
PDBsum
2fm2
PubMed
16352601
UniProt
Q9ELS8
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