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TargetGlyoxalase I
LigandBDBM50092826
Substrate/Competitorn/a
Meas. Tech.ChEMBL_424952 (CHEMBL911358)
Ki 1200±n/a nM
Citation More, SSVince, R A metabolically stable tight-binding transition-state inhibitor of glyoxalase-I. Bioorg Med Chem Lett16:6039-42 (2006) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Glyoxalase I
Name:Glyoxalase I
Synonyms:GLO1 | LGUL_YEAST | Lactoylglutathione lyase
Type:PROTEIN
Mol. Mass.:37210.98
Organism:Saccharomyces cerevisiae
Description:ChEMBL_571116
Residue:326
Sequence:
MSTDSTRYPIQIEKASNDPTLLLNHTCLRVKDPARTVKFYTEHFGMKLLSRKDFEEAKFS
LYFLSFPKDDIPKNKNGEPDVFSAHGVLELTHNWGTEKNPDYKINNGNEEPHRGFGHICF
SVSDINKTCEELESQGVKFKKRLSEGRQKDIAFALGPDGYWIELITYSREGQEYPKGSVG
NKFNHTMIRIKNPTRSLEFYQNVLGMKLLRTSEHESAKFTLYFLGYGVPKTDSVFSCESV
LELTHNWGTENDPNFHYHNGNSEPQGYGHICISCDDAGALCKEIEVKYGDKIQWSPKFNQ
GRMKNIAFLKDPDGYSIEVVPHGLIA
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  Blast E-value cutoff:
BDBM50092826
n/a
NameBDBM50092826
Synonyms:(2S)-2-amino-5-{[(1R)-1-[({[(4-bromophenyl)(hydroxy)amino]carbonyl}thio)methyl]-2-(carboxyamino)-2-oxoethyl]amino}-5-oxopentanoic acid | (S)-2-amino-5-((R)-3-((4-bromophenyl)hydroxycarbamoylthio)-1-(carboxymethylamino)-1-oxopropan-2-ylamino)-5-oxopentanoic acid | CHEMBL128872 | S-(N-4bromophenyl-N-hydroxycarbamoyl)glutathione
TypeSmall organic molecule
Emp. Form.C17H21BrN4O8S
Mol. Mass.521.34
SMILESN[C@@H](CCC(=O)N[C@@H](CSC(=O)N(O)c1ccc(Br)cc1)C(=O)NCC(O)=O)C(O)=O
Structure
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