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TargetBeta-lactamase TEM
LigandBDBM50225392
Substrate/Competitorn/a
Meas. Tech.ChEMBL_451362 (CHEMBL901565)
Ki 43±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:
BDBM50225392
n/a
NameBDBM50225392
Synonyms:5-hydroxymethylbenzo[b]thiophen-2-ylboronic acid | CHEMBL395398
TypeSmall organic molecule
Emp. Form.C8H7BO3S
Mol. Mass.194.015
SMILESOB(O)c1cc2cc(O)ccc2s1
Structure
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