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TargetAcyl-protein thioesterase 1/2
LigandBDBM50031282
Substrate/Competitorn/a
Meas. Tech.ChEMBL_100183
IC50 110000±n/a nM
Citation Mingeot-Leclercq, MPVan Schepdael, ABrasseur, RBusson, RVanderhaeghe, HJClaes, PJTulkens, PM New derivatives of kanamycin B obtained by modifications and substitutions in position 6''. 2. In vitro and computer-aided toxicological evaluation with respect to interactions with phosphatidylinositol. J Med Chem34:1476-82 (1991) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Acyl-protein thioesterase 1/2
Name:Acyl-protein thioesterase 1/2
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:24708.49
Organism:Rattus norvegicus
Description:ChEMBL_100186
Residue:230
Sequence:
MCGNNMSAPMPAVVPAARKATAAVIFLHGLGDTGHGWAEAFAGIKSSHIKYICPHAPVMP
VTLNMSMMMPSWFDIIGLSPDSQEDESGIKQAAETVKALIDQEVKNGIPSNRIILGGFSQ
GGALSLYTALTTQQKLAGVTALSCWLPLRASFSQGPINSANRDISVLQCHGDCDPLVPLM
FGSLTVERLKGLVNPANVTFKVYEGMMHSSCQQEMMDVKYFIDKLLPPID
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50031282
NameBDBM50031282
Synonyms:CHEBI:17630 | KANAMYCIN | Kanamycin
TypeSmall organic molecule
Emp. Form.C18H36N4O11
Mol. Mass.484.4986
SMILESNC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O |r|
Structure
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n/a