Structure of PDB 1jqb Chain C Binding Site BS01

Receptor Information
>1jqb Chain C (length=351) Species: 1520 (Clostridium beijerinckii) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MKGFAMLGINKLGWIEKERPVAGSYDAIVRPLAVSPCTSDIHTVFEGALG
DRKNMILGHEAVGEVVEVGSEVKDFKPGDRVIVPCTTPDWRSLEVQAGFQ
QHSNGMLAGWKFSNFKDGVFGEYFHVNDADMNLAILPKDMPLENAVMITD
MMTTGFHGAELADIEMGSSVVVIGIGAVGLMGIAGAKLRGAGRIIGVGSR
PICVEAAKFYGATDILNYKNGHIEDQVMKLTNGKGVDRVIMAGGGSETLS
QAVKMVKPGGIISNINYHGSGDALLIPRVEWGCGMAHKTIKGGLCPGGRL
RAERLRDMVVYNRVDLSKLVTHVYHGFDHIEEALLLMKDKPKDLIKAVVI
L
Ligand information
Ligand IDZN
InChIInChI=1S/Zn/q+2
InChIKeyPTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
CACTVS 3.341[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
FormulaZn
NameZINC ION
ChEMBLCHEMBL1236970
DrugBankDB14532
ZINC
PDB chain1jqb Chain C Residue 3353 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB1jqb Structural basis for the enhanced thermal stability of alcohol dehydrogenase mutants from the mesophilic bacterium Clostridium beijerinckii: contribution of salt bridging
Resolution1.97 Å
Binding residue
(original residue number in PDB)
C3037 H3059 D3150
Binding residue
(residue number reindexed from 1)
C37 H59 D150
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) D3089 S3092 V3095 S3103 D3150 T3154 K3346
Catalytic site (residue number reindexed from 1) D89 S92 V95 S103 D150 T154 K346
Enzyme Commision number 1.1.1.80: isopropanol dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0008270 zinc ion binding
GO:0016491 oxidoreductase activity
GO:0046872 metal ion binding
GO:0050009 isopropanol dehydrogenase (NADP+) activity

View graph for
Molecular Function
External links
PDB RCSB:1jqb, PDBe:1jqb, PDBj:1jqb
PDBsum1jqb
PubMed12381840
UniProtP25984|ADH_CLOBE NADP-dependent isopropanol dehydrogenase (Gene Name=adh)

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