Reaction Details |
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Target | GNAT family acetyltransferase |
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Ligand | BDBM50193478 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_385423 (CHEMBL869194) |
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Ki | 3.6±n/a nM |
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Citation | Gao, F; Yan, X; Shakya, T; Baettig, OM; Ait-Mohand-Brunet, S; Berghuis, AM; Wright, GD; Auclair, K Synthesis and structure-activity relationships of truncated bisubstrate inhibitors of aminoglycoside 6'-N-acetyltransferases. J Med Chem49:5273-81 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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GNAT family acetyltransferase |
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Name: | GNAT family acetyltransferase |
Synonyms: | Aminoglycoside acetyltransferase |
Type: | PROTEIN |
Mol. Mass.: | 21017.80 |
Organism: | Enterococcus durans |
Description: | ChEMBL_385423 |
Residue: | 183 |
Sequence: | MIISEFDRDNLVLRDQLADLLRLTWPDEYGEQPMKEVERLLEDERIAVSAIEGDELIGFV
GAIPQYGQTGWELHPLVVESMYRKQQVGTRLVSYLEKEIASQGGIVVYLGTDDVEGQTSL
AIEEDLFEDTFDKLETIQNRKDHPYEFYEKLGYQIVGVIPDANGWNKPDIWMAKRIARKH
GSE
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BDBM50193478 |
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n/a |
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Name | BDBM50193478 |
Synonyms: | CID44415032 | [(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonatooxy)oxolan-2-yl]methyl {[(3R)-3-hydroxy-2,2-dimethyl-3-{[2-({2-[({[2-(piperazin-1-yl)ethyl]carbamoyl}methyl)sulfanyl]ethyl}carbamoyl)ethyl]carbamoyl}propyl phosphonato]oxy}phosphonate | truncated aminoglycoside-coenzyme A bisubstrate analogue 4e |
Type | Small organic molecule |
Emp. Form. | C29H47N10O17P3S |
Mol. Mass. | 932.729 |
SMILES | CC(C)(COP([O-])(=O)OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1OP([O-])([O-])=O)n1cnc2c(N)ncnc12)[C@@H](O)C(=O)NCCC(=O)NCCSCC(=O)NCCN1CCNCC1 |
Structure |
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