Structure of PDB 1h1m Chain D Binding Site BS02
Receptor Information
>1h1m Chain D (length=343) Species:
34381
(Aspergillus japonicus) [
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SLIVEDAPDHVRPYVIRHYSHARAVTVDTQLYRFYVTGPSSGYAFTLMGT
NAPHSDALGVLPHIHQKHYENFYCNKGSFQLWAQSGNETQQTRVLSSGDY
GSVPRNVTHTFQIQDPDTEMTGVIVPGGFEDLFYYLGTNATDTTHTPYIP
SSSTTGPDSSTISTLQSFDVYAELSFTPRTDTVNGTAPANTVWHTGANAL
ASTAGDPYFIANGWGPKYLNSQYGYQIVAPFVTATQAQDTNYTLSTISMS
TTPSTVTVPTWSFPGACAFQVQEGRVVVQIGDYAATELGSGDVAFIPGGV
EFKYYSEAYFSKVLFVSSGSDGLDQNLVNGGEEWSSVSFPADW
Ligand information
Ligand ID
CU
InChI
InChI=1S/Cu/q+2
InChIKey
JPVYNHNXODAKFH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cu+2]
CACTVS 3.341
[Cu++]
Formula
Cu
Name
COPPER (II) ION
ChEMBL
DrugBank
DB14552
ZINC
PDB chain
1h1m Chain D Residue 1357 [
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Receptor-Ligand Complex Structure
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PDB
1h1m
Anaerobic Enzyme.Substrate Structures Provide Insight Into the Reaction Mechanism of the Copper- Dependent Quercetin 2,3-Dioxygenase.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
H66 H68 E73 H112
Binding residue
(residue number reindexed from 1)
H63 H65 E70 H109
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H66 H68 E73 H112
Catalytic site (residue number reindexed from 1)
H63 H65 E70 H109
Enzyme Commision number
1.13.11.24
: quercetin 2,3-dioxygenase.
Gene Ontology
Molecular Function
GO:0008127
quercetin 2,3-dioxygenase activity
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
View graph for
Molecular Function
External links
PDB
RCSB:1h1m
,
PDBe:1h1m
,
PDBj:1h1m
PDBsum
1h1m
PubMed
12486225
UniProt
Q7SIC2
|QDOI_ASPJA Quercetin 2,3-dioxygenase
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