Reaction Details |
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Target | Beta-lactamase TEM |
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Ligand | BDBM50282575 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_164508 |
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Ki | 50000±n/a nM |
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Citation | Martin, R; Gold, M; Jones, J Inhibition of the RTEM-1 β-lactamase by boronic acids Bioorg Med Chem Lett4:1229-1234 (1994) Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-lactamase TEM |
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Name: | Beta-lactamase TEM |
Synonyms: | BLAT_ECOLX | Bacterial beta-lactamase TEM | Beta-lactamase (TEM-1) | Beta-lactamase TEM | Beta-lactamase TEM-1 | Beta-lactamase TEM-1b | Beta-lactamase TEM1D | Beta-lactamase TEM1E | Beta-lactamase TEM1F | TEM beta lactamase | TEM extended-spectrum beta-lactamase | TEM-1 beta-lactamase | bla |
Type: | Enzyme |
Mol. Mass.: | 31512.33 |
Organism: | Escherichia coli |
Description: | P62593 |
Residue: | 286 |
Sequence: | MSIQHFRVALIPFFAAFCLPVFAHPETLVKVKDAEDQLGARVGYIELDLNSGKILESFRP
EERFPMMSTFKVLLCGAVLSRVDAGQEQLGRRIHYSQNDLVEYSPVTEKHLTDGMTVREL
CSAAITMSDNTAANLLLTTIGGPKELTAFLHNMGDHVTRLDRWEPELNEAIPNDERDTTM
PAAMATTLRKLLTGELLTLASRQQLIDWMEADKVAGPLLRSALPAGWFIADKSGAGERGS
RGIIAALGPDGKPSRIVVIYTTGSQATMDERNRQIAEIGASLIKHW
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BDBM50282575 |
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n/a |
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Name | BDBM50282575 |
Synonyms: | 2-(3-Methoxyphenyl)ethyl boronic acid | CHEMBL281783 |
Type | Small organic molecule |
Emp. Form. | C9H13BO3 |
Mol. Mass. | 180.009 |
SMILES | COc1cccc(CCB(O)O)c1 |
Structure |
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