Structure of PDB 1ugs Chain A Binding Site BS01

Receptor Information
>1ugs Chain A (length=203) Species: 1848 (Pseudonocardia thermophila) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
TENILRKSDEEIQKEITARVKALESMLIEQGILTTSMIDRMAEIYENEVG
PHLGAKVVVKAWTDPEFKKRLLADGTEACKELGIGGLQGEDMMWVENTDE
VHHVVVCTLCSCTPWPVLGLPPNWFKEPQYRSRVVREPRQLLKEEFGFEV
PPSKEIKVWDSSSEMRFVVLPQRPAGTDGWSEEELATLVTRESMIGVEPA
KAV
Ligand information
Ligand IDCO
InChIInChI=1S/Co/q+2
InChIKeyXLJKHNWPARRRJB-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Co+2]
CACTVS 3.341[Co++]
FormulaCo
NameCOBALT (II) ION
ChEMBL
DrugBankDB14205
ZINC
PDB chain1ugs Chain A Residue 301 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB1ugs Mutational and structural analysis of cobalt-containing nitrile hydratase on substrate and metal binding
Resolution2.0 Å
Binding residue
(original residue number in PDB)
C108 C111 S112 C113
Binding residue
(residue number reindexed from 1)
C107 C110 S111 C112
Annotation score1
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:1ugs, PDBe:1ugs, PDBj:1ugs
PDBsum1ugs
PubMed14717710
UniProtQ7SID2|NHAA_PSETH Cobalt-containing nitrile hydratase subunit alpha

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