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TargetBeta-lactamase TEM
LigandBDBM50022790
Substrate/Competitorn/a
Meas. Tech.ChEBML_40718
Ki 20000±n/a nM
Citation Joyeau, RMolines, HLabia, RWakselman, M N-aryl 3-halogenated azetidin-2-ones and benzocarbacephems, inhibitors of beta-lactamases. J Med Chem31:370-4 (1988) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Beta-lactamase TEM
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50022790
n/a
NameBDBM50022790
Synonyms:1-Oxo-2,2a,3,4-tetrahydro-1H-azeto[1,2-a]quinoline-7-carboxylic acid | CHEMBL333494
TypeSmall organic molecule
Emp. Form.C12H11NO3
Mol. Mass.217.2206
SMILESOC(=O)c1ccc2CCC3CC(=O)N3c2c1
Structure
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