All Stories

  1. From Obscurity to Opportunity: LpxH Emerges as a Promising Antibiotic Target in the Battle against Gram-Negative Pathogens
  2. Design and Evaluation of Pyridinyl Sulfonyl Piperazine LpxH Inhibitors with Potent Antibiotic Activity Against Enterobacterales
  3. Crystal structure of MAGEA4 MHD-RAD18 R6BD reveals a flipped binding mode compared to AlphaFold2 prediction
  4. The landscape of small-molecule prodrugs
  5. Bacterial pathogens deliver water- and solute-permeable channels to plant cells
  6. Preclinical safety and efficacy characterization of an LpxC inhibitor against Gram-negative pathogens
  7. Structure and dynamics of the Arabidopsis O-fucosyltransferase SPINDLY
  8. Structural basis of NPR1 in activating plant immunity
  9. Synthesis and evaluation of sulfonyl piperazine LpxH inhibitors
  10. MESH1 is a cytosolic NADPH phosphatase that regulates ferroptosis
  11. Structural basis of the UDP-diacylglucosamine pyrophosphohydrolase LpxH inhibition by sulfonyl piperazine antibiotics
  12. A Small Molecule Targeting Mutagenic Translesion Synthesis Improves Chemotherapy
  13. Structure–Activity Relationship of Sulfonyl Piperazine LpxH Inhibitors Analyzed by an LpxE-Coupled Malachite Green Assay
  14. Curative Treatment of Severe Gram-Negative Bacterial Infections by a New Class of Antibiotics Targeting LpxC
  15. Structure of the essential Haemophilus influenzae UDP-diacylglucosamine pyrophosphohydrolase LpxH in lipid A biosynthesis
  16. The Missing Link in C. trachomatis Lipid A Biosynthesis
  17. The UDP-diacylglucosamine Pyrophosphohydrolase LpxH in Lipid A Biosynthesis Utilizes Mn2+ Cluster for Catalysis