All Stories

  1. AI is a viable alternative to high throughput screening: a 318-target study
  2. Single-molecule FRET and molecular dynamics simulations reveal early activation steps of MET receptor byListeria monocytogenes
  3. Biochemical characterization of Mycobacterium tuberculosis dihydroorotate dehydrogenase and identification of a selective inhibitor
  4. Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5-a]pyridine Scaffold: SAR of the Aryloxyaryl Moiety
  5. Curcumin-based-fluorescent probes targeting ALDH1A3 as a promising tool for glioblastoma precision surgery and early diagnosis
  6. The integration of AlphaFold-predicted and crystal structures of human trans-3-hydroxy-l-proline dehydratase reveals a regulatory catalytic mechanism
  7. Engineering, Characterization, and Biological Evaluation of an Antibody Targeting the HGF Receptor
  8. A Selective Competitive Inhibitor of Aldehyde Dehydrogenase 1A3 Hinders Cancer Cell Growth, Invasiveness and Stemness In Vitro
  9. A highly selective electrochemical assay based on the Sakaguchi reaction for the detection of protein arginine methylation state
  10. Mycobacterium tuberculosis Pathogenesis, Infection Prevention and Treatment
  11. Structure of Thermococcus litoralis Δ1-pyrroline-2-carboxylate reductase in complex with NADH and L-proline
  12. Targeting NAD-dependent dehydrogenases in drug discovery against infectious diseases and cancer
  13. Imidazo[1,2-a]pyridine Derivatives as Aldehyde Dehydrogenase Inhibitors: Novel Chemotypes to Target Glioblastoma Stem Cells
  14. Progress in the Field of Aldehyde Dehydrogenase Inhibitors: Novel Imidazo[1,2-a]pyridines against the 1A Family
  15. Extracellular NAD+ enhances PARP-dependent DNA repair capacity independently of CD73 activity
  16. Structure of Thermococcus litoralis trans-3-hydroxy-l-proline dehydratase in the free and substrate-complexed form
  17. Synthesis and Structure–Activity relationship of 1-(5-isoquinolinesulfonyl)piperazine analogues as inhibitors of Mycobacterium tuberculosis IMPDH
  18. The Synthesis of Kynurenic Acid in Mammals: An Updated Kynurenine Aminotransferase Structural KATalogue
  19. Crystal structure of a thermophilic O6-alkylguanine-DNA alkyltransferase-derived self-labeling protein-tag in covalent complex with a fluorescent probe
  20. Hit discovery of Mycobacterium tuberculosis inosine 5′-monophosphate dehydrogenase, GuaB2, inhibitors
  21. Expanding Benzoxazole-Based Inosine 5′-Monophosphate Dehydrogenase (IMPDH) Inhibitor Structure–Activity As Potential Antituberculosis Agents
  22. Development of Potent Inhibitors of the Mycobacterium tuberculosis Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside Macrophages
  23. Mycobacterium tuberculosis Molecular Determinants of Infection, Survival Strategies, and Vulnerable Targets
  24. Design, synthesis, SAR and biological investigation of 3-(carboxymethyl)rhodanine and aminothiazole inhibitors of Mycobacterium tuberculosis Zmp1
  25. Absolute structure and structure-function relationships of 4R,2′R and 4S,2′S Pidotimod ®
  26. Structural investigations on orotate phosphoribosyltransferase from Mycobacterium tuberculosis, a key enzyme of the de novo pyrimidine biosynthesis
  27. Biochemical and structural investigations on phosphoribosylpyrophosphate synthetase from Mycobacterium smegmatis
  28. Structures of citrate synthase and malate dehydrogenase of M ycobacterium tuberculosis
  29. Discovery of the first potent and selective Mycobacterium tuberculosis Zmp1 inhibitor
  30. Crystal structure of theMycobacterium tuberculosisphosphate binding protein PstS3
  31. Single-molecule photobleaching reveals increased MET receptor dimerization upon ligand binding in intact cells
  32. Functional characterization of the Mycobacterium tuberculosis zinc metallopeptidase Zmp1 and identification of potential substrates
  33. Crystal Structure ofMycobacterium tuberculosisZinc-dependent Metalloprotease-1 (Zmp1), a Metalloprotease Involved in Pathogenicity
  34. Ligand-Mediated Dimerization of the Met Receptor Tyrosine Kinase by the Bacterial Invasion Protein InlB
  35. Structure of the Human Receptor Tyrosine Kinase Met in Complex with the Listeria Invasion Protein InlB
  36. Zinc-Dependent Metalloprotease-1 (Zmp1)