Structure of PDB 3kee Chain D Binding Site BS01
Receptor Information
>3kee Chain D (length=178) [
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ITAYSQQTRGLLGCIITSLTGRDKNQVEGEVQVVSTATQSFLATCVNGVC
WTVYHGAGSKTLAGPKGPITQMYTNVDQDLVGWQAPPGARSLTPCTCGSS
DLYLVTRHADVIPVRRRGDSRGSLLSPRPVSYLKGSSGGPLLCPSGHAVG
IFRAAVCTRGVAKAVDFVPVESMETTMR
Ligand information
>3kee Chain H (length=12) [
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KGSVVIVGRIVL
Receptor-Ligand Complex Structure
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PDB
3kee
Induced-Fit Binding of the Macrocyclic Noncovalent Inhibitor TMC435 to its HCV NS3/NS4A Protease Target
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
T4 A5 Y6 S7 Q8 Q9 T10 R11 C16 T19 S20 E30 V33 Q34 V35 V36 S37 K62 T63 L64 T108
Binding residue
(residue number reindexed from 1)
T2 A3 Y4 S5 Q6 Q7 T8 R9 C14 T17 S18 E28 V31 Q32 V33 V34 S35 K60 T61 L62 T106
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:3kee
,
PDBe:3kee
,
PDBj:3kee
PDBsum
3kee
PubMed
20166108
UniProt
P90191
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