Structure of PDB 1qh5 Chain A Binding Site BS01
Receptor Information
>1qh5 Chain A (length=260) Species:
9606
(Homo sapiens) [
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MKVEVLPALTDNYMYLVIDDETKEAAIVDPVQPQKVVDAARKHGVKLTTV
LTTHHHWDHAGGNEKLVKLESGLKVYGGDDRIGALTHKITHLSTLQVGSL
NVKCLATPCHTSGHICYFVSKPGGSEPPAVFTGDTLFVAGCGKFYEGTAD
EMCKALLEVLGRLPPDTRVYCGHEYTINNLKFARHVEPGNAAIREKLAWA
KEKYSIGEPTVPSTLAEEFTYNPFMRVREKTVQQHAGETDPVTTMRAVRR
EKDQFKMPRD
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
1qh5 Chain A Residue 261 [
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Receptor-Ligand Complex Structure
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PDB
1qh5
Crystal structure of human glyoxalase II and its complex with a glutathione thiolester substrate analogue.
Resolution
1.45 Å
Binding residue
(original residue number in PDB)
H54 H56 H110 D134
Binding residue
(residue number reindexed from 1)
H54 H56 H110 D134
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H54 H56 D58 H59 H110 D134 H173
Catalytic site (residue number reindexed from 1)
H54 H56 D58 H59 H110 D134 H173
Enzyme Commision number
3.1.2.6
: hydroxyacylglutathione hydrolase.
Gene Ontology
Molecular Function
GO:0004416
hydroxyacylglutathione hydrolase activity
Biological Process
GO:0019243
methylglyoxal catabolic process to D-lactate via S-lactoyl-glutathione
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Molecular Function
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Biological Process
External links
PDB
RCSB:1qh5
,
PDBe:1qh5
,
PDBj:1qh5
PDBsum
1qh5
PubMed
10508780
UniProt
Q16775
|GLO2_HUMAN Hydroxyacylglutathione hydrolase, mitochondrial (Gene Name=HAGH)
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