Structure of PDB 1ugp Chain A Binding Site BS01
Receptor Information
>1ugp Chain A (length=203) Species:
1848
(Pseudonocardia thermophila) [
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TENILRKSDEEIQKEITARVKALESMLIEQGILTTSMIDRMAEIYENEVG
PHLGAKVVVKAWTDPEFKKRLLADGTEACKELGIGGLQGEDMMWVENTDE
VHHVVVCTLCSCYPWPVLGLPPNWFKEPQYRSRVVREPRQLLKEEFGFEV
PPSKEIKVWDSSSEMRFVVLPQRPAGTDGWSEEELATLVTRESMIGVEPA
KAV
Ligand information
Ligand ID
CO
InChI
InChI=1S/Co/q+2
InChIKey
XLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341
[Co++]
Formula
Co
Name
COBALT (II) ION
ChEMBL
DrugBank
DB14205
ZINC
PDB chain
1ugp Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1ugp
Mutational and structural analysis of cobalt-containing nitrile hydratase on substrate and metal binding
Resolution
1.63 Å
Binding residue
(original residue number in PDB)
C108 A111 S112 C113
Binding residue
(residue number reindexed from 1)
C107 A110 S111 C112
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
C108 C111 S112 C113
Catalytic site (residue number reindexed from 1)
C107 C110 S111 C112
Enzyme Commision number
4.2.1.84
: nitrile hydratase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005515
protein binding
GO:0016829
lyase activity
GO:0018822
nitrile hydratase activity
GO:0046872
metal ion binding
GO:0046914
transition metal ion binding
GO:0050897
cobalt ion binding
GO:0080109
indole-3-acetonitrile nitrile hydratase activity
Biological Process
GO:0050899
nitrile catabolic process
Cellular Component
GO:0005575
cellular_component
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ugp
,
PDBe:1ugp
,
PDBj:1ugp
PDBsum
1ugp
PubMed
14717710
UniProt
Q7SID2
|NHAA_PSETH Cobalt-containing nitrile hydratase subunit alpha
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