Reaction Details |
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Target | Beta-lactamase |
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Ligand | BDBM50115621 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Enzyme Inhibition Assay |
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pH | 7±0 |
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Ki | 6.5e+3±n/a nM |
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Citation | Caselli, E; Powers, RA; Blasczcak, LC; Wu, CY; Prati, F; Shoichet, BK Energetic, structural, and antimicrobial analyses of beta-lactam side chain recognition by beta-lactamases. Chem Biol8:17-31 (2001) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Beta-lactamase |
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Name: | Beta-lactamase |
Synonyms: | BLAC_STAAU | Beta-lactamase TEM | Penicillinase | blaZ |
Type: | PROTEIN |
Mol. Mass.: | 31367.53 |
Organism: | Staphylococcus aureus |
Description: | ChEMBL_41052 |
Residue: | 281 |
Sequence: | MKKLIFLIVIALVLSACNSNSSHAKELNDLEKKYNAHIGVYALDTKSGKEVKFNSDKRFA
YASTSKAINSAILLEQVPYNKLNKKVHINKDDIVAYSPILEKYVGKDITLKALIEASMTY
SDNTANNKIIKEIGGIKKVKQRLKELGDKVTNPVRYEIELNYYSPKSKKDTSTPAAFGKT
LNKLIANGKLSKENKKFLLDLMLNNKSGDTLIKDGVPKDYKVADKSGQAITYASRNDVAF
VYPKGQSEPIVLVIFTNKDNKSDKPNDKLISETAKSVMKEF
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BDBM50115621 |
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n/a |
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Name | BDBM50115621 |
Synonyms: | (2-(thiophen-2-yl)acetamido)methylboronic acid | Acylglycineboronic acid, 11 | CHEMBL320049 | N-2-THIOPHEN-2-YL-ACETAMIDE BORONIC ACID | N-dihydroxyBoranylmethyl-2-thiophen-2-yl-acetamide |
Type | Small organic molecule |
Emp. Form. | C7H10BNO3S |
Mol. Mass. | 199.035 |
SMILES | OB(O)CNC(=O)Cc1cccs1 |
Structure |
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