Structure of PDB 2k1q Chain A Binding Site BS01
Receptor Information
>2k1q Chain A (length=165) [
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TGRDKNQVEGEVQVVSTATQSFLATCVNGVCWTVYHGAGSKTLAGPKGPI
TQMYTNVDQDLVGWQAPPGARSLTPCTCGSSDLYLVTRHADVIPVRRRGD
SRGSLLSPRPVSYLKGSSGGPLLCPSGHAVGIFRAAVCTRGVAKAVDFVP
VESMETTMRASKKKK
Ligand information
>2k1q Chain B (length=4) [
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ELPF
Receptor-Ligand Complex Structure
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PDB
2k1q
Binding of a noncovalent inhibitor exploiting the S' region stabilizes the hepatitis C virus NS3 protease conformation in the absence of cofactor.
Resolution
N/A
Binding residue
(original residue number in PDB)
Q41 S42 H57 G58 V132 L135 K136 G137 S139 A156 A157
Binding residue
(residue number reindexed from 1)
Q20 S21 H36 G37 V111 L114 K115 G116 S118 A135 A136
Enzymatic activity
Catalytic site (original residue number in PDB)
H57 D81 G137 S139
Catalytic site (residue number reindexed from 1)
H36 D60 G116 S118
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:2k1q
,
PDBe:2k1q
,
PDBj:2k1q
PDBsum
2k1q
PubMed
19061898
UniProt
P90191
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