Structure of PDB 1qin Chain B Binding Site BS02
Receptor Information
>1qin Chain B (length=176) Species:
9606
(Homo sapiens) [
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GGLTDEAALSCCSDADPSTKDFLLQQTMLRVKDPKKSLDFYTRVLGMTLI
QKCDFPIMKFSLYFLAYEDKNDIPKEKDEKIAWALSRKATLELTHNWGTE
DDETQSYHNGNSDPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKM
KGLAFIQDPDGYWIEILNPNKMATLM
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
1qin Chain B Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1qin
Reaction mechanism of glyoxalase I explored by an X-ray crystallographic analysis of the human enzyme in complex with a transition state analogue.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
Q33 E99
Binding residue
(residue number reindexed from 1)
Q26 E92
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Q33 E99 H126 E172
Catalytic site (residue number reindexed from 1)
Q26 E92 H119 E165
Enzyme Commision number
4.4.1.5
: lactoylglutathione lyase.
Gene Ontology
Molecular Function
GO:0004462
lactoylglutathione lyase activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016829
lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006357
regulation of transcription by RNA polymerase II
GO:0006749
glutathione metabolic process
GO:0009438
methylglyoxal metabolic process
GO:0030316
osteoclast differentiation
GO:0043066
negative regulation of apoptotic process
Cellular Component
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1qin
,
PDBe:1qin
,
PDBj:1qin
PDBsum
1qin
PubMed
10521255
UniProt
Q04760
|LGUL_HUMAN Lactoylglutathione lyase (Gene Name=GLO1)
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