All Stories

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