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Co-opting the Cell Wall in Fighting Methicillin-Resistant Staphylococcus aureus: Potent Inhibition of PBP 2a by Two Anti-MRSA β-Lactam Antibiotics

Journal of the American Chemical Society, 2008-07, Vol.130 (29), p.9212-9213

2008

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Structural Basis for Progression toward the Carbapenemase Activity in the GES Family of β‑Lactamases

Journal of the American Chemical Society, 2012-12, Vol.134 (48), p.19512-19515

2012

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The l,d-Transpeptidase Ldt Ab from Acinetobacter baumannii Is Poorly Inhibited by Carbapenems and Has a Unique Structural Architecture

ACS infectious diseases, 2022-09, Vol.8 (9), p.1948-1961

2022

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The l,d-Transpeptidase LdtAb from Acinetobacter baumannii Is Poorly Inhibited by Carbapenems and Has a Unique Structural Architecture

ACS infectious diseases, 2022-09, Vol.8 (9), p.1948-1961

2022

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Structural Consequences of the Inhibitor-Resistant Ser130Gly Substitution in TEM β-Lactamase

Biochemistry (Easton), 2005-07, Vol.44 (26), p.9330-9338

2005

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Selection and Characterization of β-Lactam–β-Lactamase Inactivator-Resistant Mutants following PCR Mutagenesis of the TEM-1 β-Lactamase Gene

Antimicrobial Agents and Chemotherapy, 1998-07, Vol.42 (7), p.1542-1548

1998

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Design of Novel Antibiotics that Bind to the Ribosomal Acyltransfer Site

Journal of the American Chemical Society, 2002-04, Vol.124 (13), p.3229-3237

2002

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Characterization of the β-Lactam Antibiotic Sensor Domain of the MecR1 Signal Sensor/Transducer Protein from Methicillin-Resistant Staphylococcus aureus

Biochemistry (Easton), 2007-07, Vol.46 (26), p.7822-7831

2007

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Synthetic Peptidoglycan Substrates for Penicillin-Binding Protein 5 of Gram-Negative Bacteria

Journal of organic chemistry, 2004-02, Vol.69 (3), p.778-784

2004

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Molecular Dynamics at the Root of Expansion of Function in the M69L Inhibitor-Resistant TEM β-Lactamase from Escherichia coli

Journal of the American Chemical Society, 2002-08, Vol.124 (32), p.9422-9430

2002

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Structural and mechanistic studies on carbapenem-hydrolysing class D serine β-lactamases leading to improved inhibitor design

Acta crystallographica. Section A, Foundations and advances, 2021-08, Vol.77 (a2), p.C104-C104

2021

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Role of the Conserved Disulfide Bridge in Class A CarbapenemasesThis work was supported by National Institutes of Health Grant R01AI089726 (to S. B. V.). The SSRL Structural Molecular Biology Program is supported by the Department of Energy Office of Biological and Environmental Research and by the National Institutes of Health, National Institute of General Medical Sciences (including Grant P41GM103393). The authors declare that they have no conflicts of interest with the contents of this artic

The Journal of biological chemistry, 2016-10, Vol.291 (42), p.22196-22206

2016

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Bulky "Gatekeeper" Residue Changes the Cosubstrate Specificity of Aminoglycoside 2 double prime -Phosphotransferase IIa

Antimicrobial agents and chemotherapy, 2013-08, Vol.57 (8), p.3763-3766

2013

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Intrinsic Class D β-Lactamases of italic toggle="yes">Clostridium difficile /italic

mBio, 2018-12, Vol.9 (6)

2018

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Molecular Dynamics at the Root of Expansion of Function in the M69L Inhibitor-Resistant TEM β-Lactamase from Escherichia c oli

Journal of the American Chemical Society, 2002-08, Vol.124 (32), p.9422-9430

2002

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Evidence for Structural Elasticity of Class A β-Lactamases in the Course of Catalytic Turnover of the Novel Cephalosporin Cefepime

Journal of the American Chemical Society, 1996-08, Vol.118 (32), p.7441-7448

1996

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Aminoglycoside 2′′-Phosphotransferase IIIa (APH(2′′)-IIIa) Prefers GTP over ATP

The Journal of biological chemistry, 2012-04, Vol.287 (16), p.12893-12903

2012

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Aminoglycoside 2′′-Phosphotransferase IIIa (APH(2′′)-IIIa) Prefers GTP over ATP: STRUCTURAL TEMPLATES FOR NUCLEOTIDE RECOGNITION IN THE BACTERIAL AMINOGLYCOSIDE-2

The Journal of biological chemistry, 2012-02, Vol.287 (16), p.12893-12903

2012

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The role of conserved surface hydrophobic residues in the carbapenemase activity of the class D [beta]-lactamases

Acta crystallographica. Section D, Biological crystallography., 2017-08, Vol.73 (8), p.692

2017

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Source of Phosphate in the Enzymic Reaction as a Point of Distinction among Aminoglycoside 2″-PhosphotransferasesS

The Journal of biological chemistry, 2009-03, Vol.284 (11), p.6690-6696

2009

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Source of Phosphate in the Enzymic Reaction as a Point of Distinction among Aminoglycoside 2â³-Phosphotransferases

The Journal of biological chemistry, 2009-03, Vol.284 (11), p.6690

2009

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Cytoplasmic-Membrane Anchoring of a Class A {szligbeta}-Lactamase and Its Capacity in Manifesting Antibiotic Resistance

Antimicrobial agents and chemotherapy, 2007-08, Vol.51 (8), p.2937-2942

2007

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Mechanistic Basis for the Emergence of Catalytic Competence against Carbapenem Antibiotics by the GES Family of Î²-Lactamases

The Journal of biological chemistry, 2009-10, Vol.284 (43), p.29509

2009

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Mechanistic Basis for the Emergence of Catalytic Competence against Carbapenem Antibiotics by the GES Family of b-Lactamases

The Journal of biological chemistry, 2009-10, Vol.284 (43)

2009

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Structure of the extended-spectrum class C [beta]-lactamase ADC-1 from Acinetobacter baumannii

Acta crystallographica. Section D, Biological crystallography., 2014-03, Vol.70 (3), p.760

2014

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Co-opting the Cell Wall in Fighting Methicillin-Resistant Staphylococcus aureus: Potent Inhibition of PBP 2a by Two Anti-MRSA β-Lactam Antibiotics

Structural Basis for Progression toward the Carbapenemase Activity in the GES Family of β‑Lactamases

The l,d-Transpeptidase Ldt Ab from Acinetobacter baumannii Is Poorly Inhibited by Carbapenems and Has a Unique Structural Architecture

The l,d-Transpeptidase LdtAb from Acinetobacter baumannii Is Poorly Inhibited by Carbapenems and Has a Unique Structural Architecture

Structural Consequences of the Inhibitor-Resistant Ser130Gly Substitution in TEM β-Lactamase

Selection and Characterization of β-Lactam–β-Lactamase Inactivator-Resistant Mutants following PCR Mutagenesis of the TEM-1 β-Lactamase Gene

Design of Novel Antibiotics that Bind to the Ribosomal Acyltransfer Site

Characterization of the β-Lactam Antibiotic Sensor Domain of the MecR1 Signal Sensor/Transducer Protein from Methicillin-Resistant Staphylococcus aureus

Synthetic Peptidoglycan Substrates for Penicillin-Binding Protein 5 of Gram-Negative Bacteria

Molecular Dynamics at the Root of Expansion of Function in the M69L Inhibitor-Resistant TEM β-Lactamase from Escherichia coli

Structural and mechanistic studies on carbapenem-hydrolysing class D serine β-lactamases leading to improved inhibitor design

Bulky "Gatekeeper" Residue Changes the Cosubstrate Specificity of Aminoglycoside 2 double prime -Phosphotransferase IIa

Intrinsic Class D β-Lactamases of italic toggle="yes">Clostridium difficile /italic

Molecular Dynamics at the Root of Expansion of Function in the M69L Inhibitor-Resistant TEM β-Lactamase from Escherichia c oli

Evidence for Structural Elasticity of Class A β-Lactamases in the Course of Catalytic Turnover of the Novel Cephalosporin Cefepime

Aminoglycoside 2′′-Phosphotransferase IIIa (APH(2′′)-IIIa) Prefers GTP over ATP

Aminoglycoside 2′′-Phosphotransferase IIIa (APH(2′′)-IIIa) Prefers GTP over ATP: STRUCTURAL TEMPLATES FOR NUCLEOTIDE RECOGNITION IN THE BACTERIAL AMINOGLYCOSIDE-2

The role of conserved surface hydrophobic residues in the carbapenemase activity of the class D [beta]-lactamases

Source of Phosphate in the Enzymic Reaction as a Point of Distinction among Aminoglycoside 2″-PhosphotransferasesS

Source of Phosphate in the Enzymic Reaction as a Point of Distinction among Aminoglycoside 2â³-Phosphotransferases

Cytoplasmic-Membrane Anchoring of a Class A {szligbeta}-Lactamase and Its Capacity in Manifesting Antibiotic Resistance

Mechanistic Basis for the Emergence of Catalytic Competence against Carbapenem Antibiotics by the GES Family of Î²-Lactamases

Mechanistic Basis for the Emergence of Catalytic Competence against Carbapenem Antibiotics by the GES Family of b-Lactamases

Structure of the extended-spectrum class C [beta]-lactamase ADC-1 from Acinetobacter baumannii

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