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TargetLactoylglutathione lyase
LigandBDBM50092824
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1524150 (CHEMBL3631235)
Ki 46±n/a nM
Citation Sang, YShi, QMo, MNi, CLi, ZLiu, BDeng, QCreighton, DJZheng, ZB Novel bivalent inhibitors with sub-nanomolar affinities towards human glyoxalase I. Bioorg Med Chem Lett25:4724-7 (2015) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lactoylglutathione lyase
Name:Lactoylglutathione lyase
Synonyms:Aldoketomutase | GLO1 | Glx I | Glyoxalase 1 (GLO1) | Glyoxalase I | Ketone-aldehyde mutase | LGUL_HUMAN | Methylglyoxalase | S-D-lactoylglutathione methylglyoxal lyase
Type:Enzyme
Mol. Mass.:20772.95
Organism:Homo sapiens (Human)
Description:Q04760
Residue:184
Sequence:
MAEPQPPSGGLTDEAALSCCSDADPSTKDFLLQQTMLRVKDPKKSLDFYTRVLGMTLIQK
CDFPIMKFSLYFLAYEDKNDIPKEKDEKIAWALSRKATLELTHNWGTEDDETQSYHNGNS
DPRGFGHIGIAVPDVYSACKRFEELGVKFVKKPDDGKMKGLAFIQDPDGYWIEILNPNKM
ATLM
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  Blast E-value cutoff:
BDBM50092824
n/a
NameBDBM50092824
Synonyms:CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamoyl)glutathione
TypeSmall organic molecule
Emp. Form.C17H21ClN4O8S
Mol. Mass.476.889
SMILESN[C@@H](CCC(=O)N[C@@H](CSC(=O)N(O)c1ccc(Cl)cc1)C(=O)NCC(O)=O)C(O)=O
Structure
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