Structure of PDB 7wsz Chain A Binding Site BS02
Receptor Information
>7wsz Chain A (length=183) Species:
9606
(Homo sapiens) [
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GGLTDEAALSCCSDADPSTKDFLLQQTMLRVKDPKKSLDFYTRVLGMTLI
QKCDFPIMKFSLYFLAYEDKNDIPKEKDEKIAWALSRKATLELTHNWGTE
DDETQSYHNGNSDPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKM
KGLAFIQDPDGYWIEILNPNKMATLMLEHHHHH
Ligand information
Ligand ID
GOL
InChI
InChI=1S/C3H8O3/c4-1-3(6)2-5/h3-6H,1-2H2
InChIKey
PEDCQBHIVMGVHV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
C(C(CO)O)O
ACDLabs 12.01
CACTVS 3.370
OCC(O)CO
Formula
C3 H8 O3
Name
GLYCEROL;
GLYCERIN;
PROPANE-1,2,3-TRIOL
ChEMBL
CHEMBL692
DrugBank
DB09462
ZINC
ZINC000000895048
PDB chain
7wsz Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
7wsz
Crystal structures of human glyoxalase I and its complex with TLSC702 reveal inhibitor binding mode and substrate preference.
Resolution
1.52 Å
Binding residue
(original residue number in PDB)
H126 M157 E172 M183
Binding residue
(residue number reindexed from 1)
H119 M150 E165 M176
Annotation score
1
Enzymatic activity
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:7wsz
,
PDBe:7wsz
,
PDBj:7wsz
PDBsum
7wsz
PubMed
35363883
UniProt
Q04760
|LGUL_HUMAN Lactoylglutathione lyase (Gene Name=GLO1)
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