1
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Clavulanic acid inactivation of SHV-1 and the inhibitor-resistant S130G SHV-1 beta-lactamase. Insights into the mechanism of inhibition.
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J Biol Chem
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2005
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1.37
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2
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Rational design of a beta-lactamase inhibitor achieved via stabilization of the trans-enamine intermediate: 1.28 A crystal structure of wt SHV-1 complex with a penam sulfone.
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J Am Chem Soc
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2006
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1.36
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3
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Different intermediate populations formed by tazobactam, sulbactam, and clavulanate reacting with SHV-1 beta-lactamases: Raman crystallographic evidence.
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J Am Chem Soc
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2009
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1.16
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4
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Design, synthesis, and crystal structures of 6-alkylidene-2'-substituted penicillanic acid sulfones as potent inhibitors of Acinetobacter baumannii OXA-24 carbapenemase.
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J Am Chem Soc
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2010
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1.12
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5
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Evaluation of penicillin-based inhibitors of the class A and B beta-lactamases from Bacillus anthracis.
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Biochem Biophys Res Commun
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2004
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1.08
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6
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Strategic design of an effective beta-lactamase inhibitor: LN-1-255, a 6-alkylidene-2'-substituted penicillin sulfone.
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J Biol Chem
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2008
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1.07
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7
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Stereoselective ketone reduction by a carbonyl reductase from Sporobolomyces salmonicolor. Substrate specificity, enantioselectivity and enzyme-substrate docking studies.
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Org Biomol Chem
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2006
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0.96
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8
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Penicillin sulfone inhibitors of class D beta-lactamases.
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Antimicrob Agents Chemother
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2010
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0.93
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9
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Ligand-dependent disorder of the Omega loop observed in extended-spectrum SHV-type beta-lactamase.
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Antimicrob Agents Chemother
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2011
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0.92
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10
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Sulbactam forms only minimal amounts of irreversible acrylate-enzyme with SHV-1 beta-lactamase.
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Biochemistry
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2007
|
0.91
|
11
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Crystal structures of KPC-2 β-lactamase in complex with 3-nitrophenyl boronic acid and the penam sulfone PSR-3-226.
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Antimicrob Agents Chemother
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2012
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0.91
|
12
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Raman crystallographic studies of the intermediates formed by Ser130Gly SHV, a beta-lactamase that confers resistance to clinical inhibitors.
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Biochemistry
|
2007
|
0.90
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13
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Evaluation of beta-lactamase inhibitors in disk tests for detection of plasmid-mediated AmpC beta-lactamases in well-characterized clinical strains of Klebsiella spp.
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J Clin Microbiol
|
2005
|
0.90
|
14
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Efficient inhibition of class A and class D beta-lactamases by Michaelis complexes.
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J Biol Chem
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2007
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0.89
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15
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Carboxylation and decarboxylation of active site Lys 84 controls the activity of OXA-24 β-lactamase of Acinetobacter baumannii: Raman crystallographic and solution evidence.
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J Am Chem Soc
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2012
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0.86
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16
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Structure-activity relationships of different beta-lactam antibiotics against a soluble form of Enterococcus faecium PBP5, a type II bacterial transpeptidase.
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Antimicrob Agents Chemother
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2005
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0.85
|
17
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Inactivation of a class A and a class C β-lactamase by 6β-(hydroxymethyl)penicillanic acid sulfone.
|
Biochem Pharmacol
|
2011
|
0.84
|
18
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Role of E166 in the imine to enamine tautomerization of the clinical beta-lactamase inhibitor sulbactam.
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Biochemistry
|
2009
|
0.82
|
19
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Early insights into the interactions of different β-lactam antibiotics and β-lactamase inhibitors against soluble forms of Acinetobacter baumannii PBP1a and Acinetobacter sp. PBP3.
|
Antimicrob Agents Chemother
|
2012
|
0.81
|
20
|
Structures of SHV-1 β-lactamase with penem and penam sulfone inhibitors that form cyclic intermediates stabilized by carbonyl conjugation.
|
PLoS One
|
2012
|
0.80
|
21
|
Approaches to the simultaneous inactivation of metallo- and serine-beta-lactamases.
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Bioorg Med Chem Lett
|
2009
|
0.79
|
22
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The importance of the trans-enamine intermediate as a β-lactamase inhibition strategy probed in inhibitor-resistant SHV β-lactamase variants.
|
ChemMedChem
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2012
|
0.79
|
23
|
Modifications of the C6-substituent of penicillin sulfones with the goal of improving inhibitor recognition and efficacy.
|
Bioorg Med Chem Lett
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2010
|
0.78
|
24
|
β-Lactamase inhibition by 7-alkylidenecephalosporin sulfones: allylic transposition and formation of an unprecedented stabilized acyl-enzyme.
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J Am Chem Soc
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2013
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0.77
|
25
|
Detecting a quasi-stable imine species on the reaction pathway of SHV-1 β-lactamase and 6β-(hydroxymethyl)penicillanic acid sulfone.
|
Biochemistry
|
2015
|
0.75
|