Reaction Details |
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Target | Methionine aminopeptidase |
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Ligand | BDBM50160054 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_305626 (CHEMBL828659) |
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IC50 | 1010±n/a nM |
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Citation | Luo, QL; Li, JY; Liu, ZY; Chen, LL; Li, J; Ye, QZ; Nan, FJ Inhibitors of type I MetAPs containing pyridine-2-carboxylic acid thiazol-2-ylamide. Part 1: SAR studies on the determination of the key scaffold. Bioorg Med Chem Lett15:635-8 (2005) [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: | EcMetAP | MAP1_ECOLI | Methionine Aminopeptidase (MAP) | Methionine aminopeptidase | Peptidase M | map |
Type: | Enzyme |
Mol. Mass.: | 29326.96 |
Organism: | Escherichia coli (strain K12) |
Description: | Full-length untagged EcMAP was expressed in E. coli. |
Residue: | 264 |
Sequence: | MAISIKTPEDIEKMRVAGRLAAEVLEMIEPYVKPGVSTGELDRICNDYIVNEQHAVSACL
GYHGYPKSVCISINEVVCHGIPDDAKLLKDGDIVNIDVTVIKDGFHGDTSKMFIVGKPTI
MGERLCRITQESLYLALRMVKPGINLREIGAAIQKFVEAEGFSVVREYCGHGIGRGFHEE
PQVLHYDSRETNVVLKPGMTFTIEPMVNAGKKEIRTMKDGWTVKTKDRSLSAQYEHTIVV
TDNGCEILTLRKDDTIPAIISHDE
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BDBM50160054 |
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n/a |
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Name | BDBM50160054 |
Synonyms: | 5-But-3-enoylamino-pyridine-2-carboxylic acid thiazol-2-ylamide | CHEMBL359929 |
Type | Small organic molecule |
Emp. Form. | C13H12N4O2S |
Mol. Mass. | 288.325 |
SMILES | C=CCC(=O)Nc1ccc(nc1)C(=O)Nc1nccs1 |
Structure |
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