All Stories

  1. Dysregulation of SIRT1, polyamines and miRNA editing in cancer and aging
  2. The Role of Metabolites in Cell–Cell Communication: A Review of Databases and Computational Tools
  3. Prophage Activation: An In Silico Platform for Identifying Prophage Regulatory Elements to Inform Phage Engineering Against Drug-Resistant Bacteria
  4. High-Efficiency Discovery and Structure–Activity-Relationship Analysis of Nonsubstrate-Based Covalent Inhibitors of S-Adenosylmethionine Decarboxylase
  5. Biological Significance and Therapeutic Promise of Programmed Ribosomal Frameshifting
  6. Subtype‐Specific Transcription Factors Affect Polyamine Metabolism and the Tumor Microenvironment in Breast Cancer
  7. High-efficiency discovery and structure-activity-relationship analysis of non-substrate-based covalent inhibitors of S-adenosylmethionine decarboxylase
  8. Structural Insights into the Mechanisms Underlying Polyaminopathies
  9. SCARdock: A Web Server and Manually Curated Resource for Discovering Covalent Ligands
  10. The computational models of AlphaFold2 and RoseTTAfold carry protein foldability information
  11. Protein-DNA complex structure modeling based on structural template
  12. The rational discovery of multipurpose inhibitors of the ornithine decarboxylase
  13. Potential covalent drugs targeting the main protease of the SARS-CoV-2 coronavirus
  14. Potential clinical drugs as covalent inhibitors of the priming proteases of the spike protein of SARS-CoV-2
  15. Electrostatic interactions in molecular recognition of intrinsically disordered proteins
  16. Polyamines Disrupt the KaiABC Oscillator by Inducing Protein Denaturation
  17. Structure-based reconstruction of a Mycobacterium hypothetical protein into an active Δ5–3-ketosteroid isomerase
  18. Intrinsically Disordered Transactivation Domains Bind to TAZ1 Domain of CBP via Diverse Mechanisms
  19. Recombinant Butelase-Mediated Cyclization of the p53-Binding Domain of the Oncoprotein MdmX-Stabilized Protein Conformation as a Promising Model for Structural Investigation
  20. The influence of intrinsic folding mechanism of an unfolded protein on the coupled folding-binding process during target recognition
  21. The influence of KaiA mutations on its function in the KaiABC circadian clock system
  22. Kallikrein-related peptidase 7 is a potential target for the treatment of pancreatic cancer
  23. The reversible function switching of the circadian clock protein KaiA is encoded in its structure
  24. 3D-quantitative structure-activity relationship and docking studies of coumarin derivatives as tissue kallikrein 7 inhibitors
  25. Expression and Purification of Cyanobacterial Circadian Clock Protein KaiC and Determination of Its Auto-phosphatase Activity
  26. Discovery of Covalent Ligands via Noncovalent Docking by Dissecting Covalent Docking Based on a “Steric-Clashes Alleviating Receptor (SCAR)” Strategy
  27. A dynamic interaction process between KaiA and KaiC is critical to the cyanobacterial circadian oscillator
  28. Two Sensitive Fluorescent BOPIM Probes with Tunable TICT Character for Low-Level Water Detection in Organic Solvents
  29. Discovery of novel inhibitors of human S-adenosylmethionine decarboxylase based on in silico high-throughput screening and a non-radioactive enzymatic assay
  30. Reliable cell cycle commitment in budding yeast is ensured by signal integration
  31. The P2/P2′ sites affect the substrate cleavage of TNF-α converting enzyme (TACE)
  32. Analysis of the Sequence Conservation of the Circadian Clock Protein KaiC
  33. Advances in the Molecular Mechanism of the Core Circadian Oscillator of Cyanobacteria
  34. Evolution Analysis of the Circadian Clock Protein KaiB
  35. Control of protein signaling using a computationally designed GTPase/GEF orthogonal pair
  36. Nonnatural protein–protein interaction-pair design by key residues grafting
  37. Expression, purification, crystallization and preliminary crystallographic study of a potential metal-dependent hydrolase with cyclase activity fromThermoanaerobacter tengcongensis