Structure of PDB 1oj7 Chain D Binding Site BS02
Receptor Information
>1oj7 Chain D (length=390) Species:
83333
(Escherichia coli K-12) [
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KAGLNNFNLHTPTRILFGKGAIAGLREQIPHDARVLITYGGGSVKKTGVL
DQVLDALKGMDVLEFGGIEPNPAYETLMNAVKLVREQKVTFLLAVGGGSV
LDGTKFIAAAANYPENIDPWHILQTGGKEIKSAIPMGCVLTLPATGSESN
AGAVISRKTTGDKQAFHSAHVQPVFAVLDPVYTYTLPPRQVANGVVDAFV
HTVEQYVTKPVDAKIHDRFAEGILLTLIEDGPKALKEPENYDVRANVMWA
ATQALNGLIGAGVPQDWATHMLGHELTAMHGLDHAQTLAIVLPALWNEKR
DTKRAKLLQYAERVWNITEGSDDERIDAAIAATRNFFEQLGVPTHLSDYG
LDGSSIPALLKKLEEHGMTQLGENHDITLDVSRRIYEAAR
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1oj7 Chain D Residue 1389 [
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Receptor-Ligand Complex Structure
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PDB
1oj7
Crystal Structure of E.Coli Alcohol Dehydrogenase Yqhd: Evidence of a Covalently Modified Nadp Coenzyme
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
D194 H198 H267 H281
Binding residue
(residue number reindexed from 1)
D197 H201 H270 H284
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.1.1.2
: alcohol dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0008106
alcohol dehydrogenase (NADP+) activity
GO:0008270
zinc ion binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0018455
alcohol dehydrogenase [NAD(P)+] activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:1990002
methylglyoxal reductase (NADPH) (acetol producing) activity
GO:1990362
butanol dehydrogenase (NAD+) activity
Biological Process
GO:0000302
response to reactive oxygen species
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1oj7
,
PDBe:1oj7
,
PDBj:1oj7
PDBsum
1oj7
PubMed
15327949
UniProt
Q46856
|YQHD_ECOLI Alcohol dehydrogenase YqhD (Gene Name=yqhD)
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