Item Type | Name |
Concept
|
Toxin-Antitoxin Systems
|
Concept
|
Amino Acid Sequence
|
Concept
|
Binding Sites
|
Concept
|
Drug Screening Assays, Antitumor
|
Concept
|
Nucleic Acid Conformation
|
Concept
|
Microbial Sensitivity Tests
|
Concept
|
Molecular Sequence Data
|
Concept
|
Molecular Structure
|
Concept
|
Signal Transduction
|
Concept
|
Staphylococcal Infections
|
Concept
|
Staphylococcus
|
Concept
|
Staphylococcus aureus
|
Concept
|
Stereoisomerism
|
Concept
|
Structure-Activity Relationship
|
Concept
|
Substrate Specificity
|
Concept
|
Protein Structure, Secondary
|
Concept
|
Protein Structure, Tertiary
|
Concept
|
Sequence Alignment
|
Concept
|
Genome, Bacterial
|
Concept
|
Genome, Archaeal
|
Concept
|
Protein Structure, Quaternary
|
Concept
|
Space Flight
|
Concept
|
United States
|
Concept
|
Chemistry Techniques, Synthetic
|
Concept
|
Structural Homology, Protein
|
Concept
|
High-Throughput Screening Assays
|
Concept
|
National Institute of Allergy and Infectious Diseases (U.S.)
|
Concept
|
Molecular Docking Simulation
|
Academic Article
|
Crystal structure of Bacillus anthracis dihydrofolate reductase with the dihydrophthalazine-based trimethoprim derivative RAB1 provides a structural explanation of potency and selectivity.
|
Academic Article
|
Synthesis and biological activity of substituted 2,4-diaminopyrimidines that inhibit Bacillus anthracis.
|
Academic Article
|
The structure and competitive substrate inhibition of dihydrofolate reductase from Enterococcus faecalis reveal restrictions to cofactor docking.
|
Academic Article
|
Comparison of the three-dimensional structures of a human Bence-Jones dimer crystallized on Earth and aboard US Space Shuttle Mission STS-95.
|
Academic Article
|
Inhibition of antibiotic-resistant Staphylococcus aureus by the broad-spectrum dihydrofolate reductase inhibitor RAB1.
|
Academic Article
|
Classifying compound mechanism of action for linking whole cell phenotypes to molecular targets.
|
Academic Article
|
Inhibition of bacterial dihydrofolate reductase by 6-alkyl-2,4-diaminopyrimidines.
|
Academic Article
|
Synthesis and biological evaluation of 2,4-diaminopyrimidine-based antifolate drugs against Bacillus anthracis.
|
Academic Article
|
Identification of novel potential antibiotics against Staphylococcus using structure-based drug screening targeting dihydrofolate reductase.
|
Academic Article
|
Modified 2,4-diaminopyrimidine-based dihydrofolate reductase inhibitors as potential drug scaffolds against Bacillus anthracis.
|
Academic Article
|
Evaluation of New Dihydrophthalazine-Appended 2,4-Diaminopyrimidines against Bacillus anthracis: Improved Syntheses Using a New Pincer Complex.
|
Academic Article
|
Inhibitor design to target a unique feature in the folate pocket of Staphylococcus aureus dihydrofolate reductase.
|
Academic Article
|
Identifying a Molecular Mechanism That Imparts Species-Specific Toxicity to YoeB Toxins.
|
Academic Article
|
A heteroaryldihydropyrimidine activates and can misdirect hepatitis B virus capsid assembly.
|
Academic Article
|
Structure-activity relationship for enantiomers of potent inhibitors of B. anthracis dihydrofolate reductase.
|
Academic Article
|
Comparative Study of the Frech Catalyst with Two Conventional Catalysts in the Heck Synthesis of 2,4-Diaminopyrimidine-based Antibiotics.
|
Academic Article
|
Microwave-assisted Heck Synthesis of Substituted 2,4-Diaminopyrimidine-based Antibiotics.
|
Academic Article
|
Toxin-Antitoxin Modules Are Pliable Switches Activated by Multiple Protease Pathways.
|
Academic Article
|
The toxin from a ParDE toxin-antitoxin system found in Pseudomonas aeruginosa offers protection to cells challenged with anti-gyrase antibiotics.
|
Academic Article
|
Evaluating the Potential for Cross-Interactions of Antitoxins in Type II TA Systems.
|
Academic Article
|
Crystal structure of a glycosylated Fab from an IgM cryoglobulin with properties of a natural proteolytic antibody.
|
Academic Article
|
Global structural changes in hepatitis B virus capsids induced by the assembly effector HAP1.
|
Academic Article
|
In vitro screening for molecules that affect virus capsid assembly (and other protein association reactions).
|
Academic Article
|
Small-molecule effectors of hepatitis B virus capsid assembly give insight into virus life cycle.
|
Academic Article
|
A mutant hepatitis B virus core protein mimics inhibitors of icosahedral capsid self-assembly.
|
Academic Article
|
High-throughput screening of a diversity collection using biodefense category A and B priority pathogens.
|
Academic Article
|
Utility of the Biosynthetic Folate Pathway for Targets in Antimicrobial Discovery.
|
Academic Article
|
Bacterial Growth Mindset: Structural Plasticity in Defense Systems.
|
Academic Article
|
A YoeB toxin cleaves both RNA and DNA.
|
Academic Article
|
Molecular Basis for the Substrate Promiscuity of Isopentenyl Phosphate Kinase from Candidatus methanomethylophilus alvus.
|
Academic Article
|
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.
|