Reaction Details |
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Target | Thiosulfate sulfurtransferase |
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Ligand | BDBM50370232 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1797977 (CHEMBL4270094) |
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IC50 | >100000±n/a nM |
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Citation | Kunkle, T; Abdeen, S; Salim, N; Ray, AM; Stevens, M; Ambrose, AJ; Victorino, J; Park, Y; Hoang, QQ; Chapman, E; Johnson, SM Hydroxybiphenylamide GroEL/ES Inhibitors Are Potent Antibacterials against Planktonic and Biofilm Forms of Staphylococcus aureus. J Med Chem61:10651-10664 (2018) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Thiosulfate sulfurtransferase |
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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
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BDBM50370232 |
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n/a |
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Name | BDBM50370232 |
Synonyms: | BA-41166E | L-5103 | RIFAMPIN | Rifadin | Rifampicin |
Type | Small organic molecule |
Emp. Form. | C43H58N4O12 |
Mol. Mass. | 822.9402 |
SMILES | CO[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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