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TargetLactoylglutathione lyase
LigandBDBM50069025
Substrate/Competitorn/a
Meas. Tech.ChEMBL_71304 (CHEMBL686107)
IC50 209600±n/a nM
Citation Ly, HDClugston, SLSampson, PBHonek, JF Syntheses and kinetic evaluation of hydroxamate-based peptide inhibitors of glyoxalase I. Bioorg Med Chem Lett8:705-10 (1999) [PubMed]
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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BDBM50069025
n/a
NameBDBM50069025
Synonyms:2-Amino-4-[1-(carboxymethyl-carbamoyl)-3-hydroxycarbamoyl-propylcarbamoyl]-butyric acid anion | CHEMBL164263
TypeSmall organic molecule
Emp. Form.C12H20N4O8
Mol. Mass.348.3092
SMILES[NH3+]C(CCC(=O)NC(CCC(=O)NO)C(=O)NCC(O)=O)C([O-])=O
Structure
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