Structure of PDB 3kf2 Chain B Binding Site BS01
Receptor Information
>3kf2 Chain B (length=181) [
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APITAYAQQTRGLLGCIITSLTGRDKNQVEGEVQIVSTATQTFLATCING
VCWTVYHGAGTRTIASPKGPVIQMYTNVDQDLVGWPAPQGSRSLTPCTCG
SSDLYLVTRHADVIPVRRRGDSRGSLLSPRPISYLKGSSGGPLLCPAGHA
VGLFRAAVCTRGVAKAVDFIPVENLETTMRS
Ligand information
>3kf2 Chain C (length=16) [
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GSVVIVGRIVLSGKPA
Receptor-Ligand Complex Structure
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PDB
3kf2
Induced-Fit Binding of the Macrocyclic Noncovalent Inhibitor TMC435 to its HCV NS3/NS4A Protease Target
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
T4 A5 Y6 A7
Binding residue
(residue number reindexed from 1)
T4 A5 Y6 A7
Enzymatic activity
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:3kf2
,
PDBe:3kf2
,
PDBj:3kf2
PDBsum
3kf2
PubMed
20166108
UniProt
B2Y2M9
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