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Escherichia coli cells evade inducible parE toxin expression by reducing plasmid copy number

Microbiology spectrum, 2024-06, Vol.12 (6), p.e0397323

2024

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Toxin-Antitoxin Modules Are Pliable Switches Activated by Multiple Protease Pathways

Toxins, 2016-07, Vol.8 (7), p.214

2016

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A YoeB toxin cleaves both RNA and DNA

Scientific reports, 2021-02, Vol.11 (1), p.3592-9, Article 3592

2021

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Friend or Foe: Protein Inhibitors of DNA Gyrase

Biology (Basel, Switzerland), 2024-01, Vol.13 (2), p.84

2024

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Utility of the Biosynthetic Folate Pathway for Targets in Antimicrobial Discovery

Antibiotics, 2014-01, Vol.3 (1), p.1-28

Bourne, Christina R

2014

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Global Structural Changes in Hepatitis B Virus Capsids Induced by the Assembly Effector HAP1

Journal of Virology, 2006-11, Vol.80 (22), p.11055-11061

2006

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A Heteroaryldihydropyrimidine Activates and Can Misdirect Hepatitis B Virus Capsid Assembly

Proceedings of the National Academy of Sciences - PNAS, 2005-06, Vol.102 (23), p.8138-8143

2005

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Identifying a Molecular Mechanism That Imparts Species-Specific Toxicity to YoeB Toxins

Frontiers in microbiology, 2020-05, Vol.11, p.959-959

2020

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Bacterial Growth Mindset: Structural Plasticity in Defense Systems

Structure (London), 2021-02, Vol.29 (2), p.97-98

Bourne, Christina R

2021

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Identification of Novel Potential Antibiotics against Staphylococcus Using Structure-Based Drug Screening Targeting Dihydrofolate Reductase

Journal of chemical information and modeling, 2014-04, Vol.54 (4), p.1242-1253

2014

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Expression of different ParE toxins results in conserved phenotypes with distinguishable classes of toxicity

MicrobiologyOpen (Weinheim), 2019-10, Vol.8 (10), p.e902-n/a

2019

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Crystal Structure of Bacillus anthracis Dihydrofolate Reductase with the Dihydrophthalazine-Based Trimethoprim Derivative RAB1 Provides a Structural Explanation of Potency and Selectivity

Antimicrobial Agents and Chemotherapy, 2009-07, Vol.53 (7), p.3065-3073

2009

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ParD Antitoxin Hotspot Alters a Disorder-to-Order Transition upon Binding to Its Cognate ParE Toxin, Lessening Its Interaction Affinity and Increasing Its Protease Degradation Kinetics

Biochemistry (Easton), 2022-01, Vol.61 (1), p.34-45

2022

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The toxin from a ParDE toxin‐antitoxin system found in Pseudomonas aeruginosa offers protection to cells challenged with anti‐gyrase antibiotics

Molecular microbiology, 2019-02, Vol.111 (2), p.441-454

2019

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Evaluation of New Dihydrophthalazine-Appended 2,4-Diaminopyrimidines against Bacillus anthracis: Improved Syntheses Using a New Pincer Complex

Molecules (Basel, Switzerland), 2015-04, Vol.20 (4), p.7222-7244

2015

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Synthesis and biological evaluation of 2,4-diaminopyrimidine-based antifolate drugs against Bacillus anthracis

Molecules (Basel, Switzerland), 2014-03, Vol.19 (3), p.3231-3246

2014

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Molecular Basis for the Substrate Promiscuity of Isopentenyl Phosphate Kinase from Candidatus methanomethylophilus alvus

ACS chemical biology, 2022-01, Vol.17 (1), p.85-102

2022

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Crystal structure of a glycosylated Fab from an IgM cryoglobulin with properties of a natural proteolytic antibody

Biochemical journal, 2006-05, Vol.395 (3), p.473-481

2006

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Inhibitor design to target a unique feature in the folate pocket of Staphylococcus aureus dihydrofolate reductase

European journal of medicinal chemistry, 2020-08, Vol.200, p.112412-112412, Article 112412

2020

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Structure–Activity Relationships of Ligand Binding to Oxysterol-Binding Protein (OSBP) and OSBP-Related Protein 4

Journal of medicinal chemistry, 2023-03, Vol.66 (6), p.3866-3875

2023

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A Mutant Hepatitis B Virus Core Protein Mimics Inhibitors of Icosahedral Capsid Self-Assembly

Biochemistry (Easton), 2009-03, Vol.48 (8), p.1736-1742

2009

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Synthesis and Characterization of Functionalized Amino Dihydropyrimidines Toward the Analysis of their Antibacterial Structure–Activity Relationships and Mechanism of Action

ACS omega, 2022-10, Vol.7 (42), p.37907-37916

2022

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Synthesis and biological activity of substituted 2,4-diaminopyrimidines that inhibit Bacillus anthracis

European journal of medicinal chemistry, 2012-08, Vol.54, p.387-396

2012

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Modified 2,4-diaminopyrimidine-based dihydrofolate reductase inhibitors as potential drug scaffolds against Bacillus anthracis

Bioorganic & medicinal chemistry, 2015-01, Vol.23 (1), p.203-211

2015

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The Structure and Competitive Substrate Inhibition of Dihydrofolate Reductase from Enterococcus faecalis Reveal Restrictions to Cofactor Docking

Biochemistry (Easton), 2014-02, Vol.53 (7), p.1228-1238

2014

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Escherichia coli cells evade inducible parE toxin expression by reducing plasmid copy number

Toxin-Antitoxin Modules Are Pliable Switches Activated by Multiple Protease Pathways

A YoeB toxin cleaves both RNA and DNA

Friend or Foe: Protein Inhibitors of DNA Gyrase

Utility of the Biosynthetic Folate Pathway for Targets in Antimicrobial Discovery

Global Structural Changes in Hepatitis B Virus Capsids Induced by the Assembly Effector HAP1

A Heteroaryldihydropyrimidine Activates and Can Misdirect Hepatitis B Virus Capsid Assembly

Identifying a Molecular Mechanism That Imparts Species-Specific Toxicity to YoeB Toxins

Bacterial Growth Mindset: Structural Plasticity in Defense Systems

Identification of Novel Potential Antibiotics against Staphylococcus Using Structure-Based Drug Screening Targeting Dihydrofolate Reductase

Expression of different ParE toxins results in conserved phenotypes with distinguishable classes of toxicity

Crystal Structure of Bacillus anthracis Dihydrofolate Reductase with the Dihydrophthalazine-Based Trimethoprim Derivative RAB1 Provides a Structural Explanation of Potency and Selectivity

ParD Antitoxin Hotspot Alters a Disorder-to-Order Transition upon Binding to Its Cognate ParE Toxin, Lessening Its Interaction Affinity and Increasing Its Protease Degradation Kinetics

The toxin from a ParDE toxin‐antitoxin system found in Pseudomonas aeruginosa offers protection to cells challenged with anti‐gyrase antibiotics

Evaluation of New Dihydrophthalazine-Appended 2,4-Diaminopyrimidines against Bacillus anthracis: Improved Syntheses Using a New Pincer Complex

Synthesis and biological evaluation of 2,4-diaminopyrimidine-based antifolate drugs against Bacillus anthracis

Molecular Basis for the Substrate Promiscuity of Isopentenyl Phosphate Kinase from Candidatus methanomethylophilus alvus

Crystal structure of a glycosylated Fab from an IgM cryoglobulin with properties of a natural proteolytic antibody

Inhibitor design to target a unique feature in the folate pocket of Staphylococcus aureus dihydrofolate reductase

Structure–Activity Relationships of Ligand Binding to Oxysterol-Binding Protein (OSBP) and OSBP-Related Protein 4

A Mutant Hepatitis B Virus Core Protein Mimics Inhibitors of Icosahedral Capsid Self-Assembly

Synthesis and Characterization of Functionalized Amino Dihydropyrimidines Toward the Analysis of their Antibacterial Structure–Activity Relationships and Mechanism of Action

Synthesis and biological activity of substituted 2,4-diaminopyrimidines that inhibit Bacillus anthracis

Modified 2,4-diaminopyrimidine-based dihydrofolate reductase inhibitors as potential drug scaffolds against Bacillus anthracis

The Structure and Competitive Substrate Inhibition of Dihydrofolate Reductase from Enterococcus faecalis Reveal Restrictions to Cofactor Docking

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