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TargetBeta-lactamase
LigandBDBM50053183
Substrate/Competitorn/a
Meas. Tech.ChEMBL_40245 (CHEMBL654925)
IC50 1800±n/a nM
Citation Richter, HGAngehrn, PHubschwerlen, CKania, MPage, MGSpecklin, JLWinkler, FK Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases. J Med Chem39:3712-22 (1996) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Beta-lactamase
Name:Beta-lactamase
Synonyms:BLAC_BACLI | blaP | penP
Type:PROTEIN
Mol. Mass.:33993.80
Organism:Bacillus licheniformis
Description:ChEMBL_571690
Residue:307
Sequence:
MKLWFSTLKLKKAAAVLLFSCVALAGCANNQTNASQPAEKNEKTEMKDDFAKLEEQFDAK
LGIFALDTGTNRTVAYRPDERFAFASTIKALTVGVLLQQKSIEDLNQRITYTRDDLVNYN
PITEKHVDTGMTLKELADASLRYSDNAAQNLILKQIGGPESLKKELRKIGDEVTNPERFE
PELNEVNPGETQDTSTARALVTSLRAFALEDKLPSEKRELLIDWMKRNTTGDALIRAGVP
DGWEVADKTGAASYGTRNDIAIIWPPKGDPVVLAVLSSRDKKDAKYDDKLIAEATKVVMK
ALNMNGK
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  Blast E-value cutoff:
BDBM50053183
n/a
NameBDBM50053183
Synonyms:CHEMBL123481 | Trifluoro-methanesulfonate1-[(E)-3-((2S,3S,5R)-2-carboxy-3-methyl-4,4,7-trioxo-4lambda*6*-thia-1-aza-bicyclo[3.2.0]hept-3-yl)-allyl]-pyridinium;
TypeSmall organic molecule
Emp. Form.C15H17N2O5S
Mol. Mass.337.37
SMILESC[C@]1(\C=C\C[n+]2ccccc2)[C@@H](N2[C@@H](CC2=O)S1(=O)=O)C(O)=O
Structure
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