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TargetThiosulfate sulfurtransferase
LigandBDBM50370232
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1797977 (CHEMBL4270094)
IC50>100000±n/a nM
Citation Kunkle, TAbdeen, SSalim, NRay, AMStevens, MAmbrose, AJVictorino, JPark, YHoang, QQChapman, EJohnson, SM Hydroxybiphenylamide GroEL/ES Inhibitors Are Potent Antibacterials against Planktonic and Biofilm Forms of Staphylococcus aureus. J Med Chem61:10651-10664 (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:
BDBM50370232
n/a
NameBDBM50370232
Synonyms:BA-41166E | L-5103 | RIFAMPIN | Rifadin | Rifampicin
TypeSmall organic molecule
Emp. Form.C43H58N4O12
Mol. Mass.822.9402
SMILESCO[C@H]1\C=C\O[C@@]2(C)Oc3c(C2=O)c2c(O)c(\C=N\N4CCN(C)CC4)c(NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)c(O)c2c(O)c3C |r,c:33,t:3,35|
Structure
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