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TargetBeta-lactamase TEM
LigandBDBM50225385
Substrate/Competitorn/a
Meas. Tech.ChEMBL_451362 (CHEMBL901565)
Ki 800±n/a nM
Citation Venturelli, ATondi, DCancian, LMorandi, FCannazza, GSegatore, BPrati, FAmicosante, GShoichet, BKCosti, MP Optimizing cell permeation of an antibiotic resistance inhibitor for improved efficacy. J Med Chem50:5644-54 (2007) [PubMed]  Article
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:
BDBM50225385
n/a
NameBDBM50225385
Synonyms:CHEMBL391537 | pinacol 5-[(4-morpholin-4-yl-phenylamino)methyl]benzo[b]-thiophen-2-ylboronate
TypeSmall organic molecule
Emp. Form.C19H21BN2O3S
Mol. Mass.368.258
SMILESOB(O)c1cc2cc(CNc3ccc(cc3)N3CCOCC3)ccc2s1
Structure
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