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TargetLactoylglutathione lyase
LigandBDBM50069026
Substrate/Competitorn/a
Meas. Tech.ChEMBL_71304 (CHEMBL686107)
IC50 140500±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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BDBM50069026
n/a
NameBDBM50069026
Synonyms:2-Amino-4-[1-(ethoxycarbonylmethyl-carbamoyl)-3-(hydroxy-methyl-carbamoyl)-propylcarbamoyl]-butyric acid anion | CHEMBL164262
TypeSmall organic molecule
Emp. Form.C15H26N4O8
Mol. Mass.390.3889
SMILESCCOC(=O)CNC(=O)C(CCC(=O)N(C)O)NC(=O)CCC([NH3+])C([O-])=O
Structure
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