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TargetThiosulfate sulfurtransferase
LigandBDBM50450012
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1741629 (CHEMBL4157379)
IC50 53000±n/a nM
Citation Abdeen, SKunkle, TSalim, NRay, AMMammadova, NSummers, CStevens, MAmbrose, AJPark, YSchultz, PGHorwich, ALHoang, QQChapman, EJohnson, SM Sulfonamido-2-arylbenzoxazole GroEL/ES Inhibitors as Potent Antibacterials against Methicillin-Resistant Staphylococcus aureus (MRSA). J Med Chem61:7345-7357 (2018) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Thiosulfate sulfurtransferase
Name:Thiosulfate sulfurtransferase
Synonyms:2.8.1.1 | Rhodanese | THTR_HUMAN | TST | Thiosulfate sulfurtransferase
Type:PROTEIN
Mol. Mass.:33432.06
Organism:Homo sapiens
Description:ChEMBL_118080
Residue:297
Sequence:
MVHQVLYRALVSTKWLAESIRTGKLGPGLRVLDASWYSPGTREARKEYLERHVPGASFFD
IEECRDTASPYEMMLPSEAGFAEYVGRLGISNHTHVVVYDGEHLGSFYAPRVWWMFRVFG
HRTVSVLNGGFRNWLKEGHPVTSEPSRPEPAVFKATLDRSLLKTYEQVLENLESKRFQLV
DSRSQGRFLGTEPEPDAVGLDSGHIRGAVNMPFMDFLTEDGFEKGPEELRALFQTKKVDL
SQPLIATCRKGVTACHVALAAYLCGKPDVAVYDGSWSEWFRRAPPESRVSQGKSEKA
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50450012
n/a
NameBDBM50450012
Synonyms:CHEMBL4167333
TypeSmall organic molecule
Emp. Form.C23H14Cl2N4O7S3
Mol. Mass.625.481
SMILES[O-][N+](=O)c1cc(ccc1Cl)S(=O)(=O)Nc1ccc(cc1)-c1nc2cc(NS(=O)(=O)c3ccc(Cl)s3)ccc2o1
Structure
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