Reaction Details |
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Target | Methionine aminopeptidase |
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Ligand | BDBM50497533 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1437717 (CHEMBL3382364) |
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IC50 | 13300±n/a nM |
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Citation | Altmeyer, M; Amtmann, E; Heyl, C; Marschner, A; Scheidig, AJ; Klein, CD Beta-aminoketones as prodrugs for selective irreversible inhibitors of type-1 methionine aminopeptidases. Bioorg Med Chem Lett24:5310-4 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Methionine aminopeptidase |
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Name: | Methionine aminopeptidase |
Synonyms: | MAP1_STAAW | MetAP | Methionine Aminopeptidase (MAP) | Peptidase M | SaMetAP-1 | map |
Type: | Enzyme |
Mol. Mass.: | 27494.40 |
Organism: | Staphylococcus aureus |
Description: | P0A079 |
Residue: | 252 |
Sequence: | MIVKTEEELQALKEIGYICAKVRNTMQAATKPGITTKELDNIAKELFEEYGAISAPIHDE
NFPGQTCISVNEEVAHGIPSKRVIREGDLVNIDVSALKNGYYADTGISFVVGESDDPMKQ
KVCDVATMAFENAIAKVKPGTKLSNIGKAVHNTARQNDLKVIKNLTGHGVGLSLHEAPAH
VLNYFDPKDKTLLTEGMVLAIEPFISSNASFVTEGKNEWAFETSDKSFVAQIEHTVIVTK
DGPILTTKIEEE
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BDBM50497533 |
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n/a |
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Name | BDBM50497533 |
Synonyms: | CHEMBL3337746 |
Type | Small organic molecule |
Emp. Form. | C11H10O |
Mol. Mass. | 158.1965 |
SMILES | Cc1ccc2C(=O)C(=C)Cc2c1 |
Structure |
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