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TargetGlyoxalase I
LigandBDBM50195360
Substrate/Competitorn/a
Meas. Tech.ChEMBL_571116 (CHEMBL1030416)
Ki 2190±n/a nM
Citation More, SSVince, R Inhibition of glyoxalase I: the first low-nanomolar tight-binding inhibitors. J Med Chem52:4650-6 (2009) [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:
BDBM50195360
n/a
NameBDBM50195360
Synonyms:(2S)-2-amino-3-[({[(1R)-1-[({[(4-bromophenyl)(hydroxy)amino]carbonyl}thio)methyl]-2-(carboxyamino)-2-oxoethyl]amino}carbonyl)amino]propanoic acid | (S)-2-amino-3-(3-((R)-3-((4-bromophenyl)hydroxycarbamoylthio)-1-(carboxymethylamino)-1-oxopropan-2-yl)ureido)propanoic acid | CHEMBL221011
TypeSmall organic molecule
Emp. Form.C16H20BrN5O8S
Mol. Mass.522.328
SMILESN[C@@H](CNC(=O)N[C@@H](CSC(=O)N(O)c1ccc(Br)cc1)C(=O)NCC(O)=O)C(O)=O
Structure
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