All Stories

  1. Crystal structure of glycerol kinase from Trypanosoma cruzi, a potential molecular target in Chagas disease
  2. Development of Chemical Tools to Monitor Human Kallikrein 13 (KLK13) Activity
  3. Development of a novel, high-affinity ssDNA trypsin inhibitor
  4. Crystal structure of the FAS1 domain of the hyaluronic acid receptor stabilin-2
  5. Structural basis for ADP-dependent glucokinase inhibition by 8-bromo–substituted adenosine nucleotide
  6. Identification of small-molecule inhibitors of USP2a
  7. Unique Substrate Specificity of SplE Serine Protease from Staphylococcus aureus
  8. A novel, dual pan-PIM/FLT3 inhibitor SEL24 exhibits broad therapeutic potential in acute myeloid leukemia
  9. Crystal structure of ADP-dependent glucokinase from Methanocaldococcus jannaschii in complex with 5-iodotubercidin reveals phosphoryl transfer mechanism
  10. Spatial attributes of the four-helix bundle group of bacteriocins – The high-resolution structure of BacSp222 in solution
  11. Modular endolysin of Burkholderia AP3 phage has the largest lysozyme-like catalytic subunit discovered to date and no catalytic aspartate residue
  12. Identification of novel mazEF/pemIK family toxin-antitoxin loci and their distribution in the Staphylococcus genus
  13. Structural analysis of PIM1 kinase complexes with ATP-competitive inhibitors
  14. Staphylococcus Aureus V8 protease disrupts the integrity of the airway epithelial barrier and impairs IL-6 production in vitro
  15. Properties of halogenated and sulfonated porphyrins relevant for the selection of photosensitizers in anticancer and antimicrobial therapies
  16. Bioactive Macrocyclic Inhibitors of the PD-1/PD-L1 Immune Checkpoint
  17. Small-molecule inhibitors of PD-1/PD-L1 immune checkpoint alleviate the PD-L1-induced exhaustion of T-cells
  18. Structural Biology of the Immune Checkpoint Receptor PD-1 and Its Ligands PD-L1/PD-L2
  19. Crystal structure of a low molecular weight activator Blm-pep with yeast 20S proteasome – insights into the enzyme activation mechanism
  20. Small-Molecule Inhibitors of the Programmed Cell Death-1/Programmed Death-Ligand 1 (PD-1/PD-L1) Interaction via Transiently Induced Protein States and Dimerization of PD-L1
  21. Malassezia globosa Mg MDL2 lipase: Crystal structure and rational modification of substrate specificity
  22. 1,4,5-Trisubstituted Imidazole-Based p53–MDM2/MDMX Antagonists with Aliphatic Linkers for Conjugation with Biological Carriers
  23. Lithocholic Acid Hydroxyamide Destabilizes Cyclin D1 and Induces G 0 /G 1 Arrest by Inhibiting Deubiquitinase USP2a
  24. Structural Characterization of Human Coronavirus NL63 N Protein
  25. Rational design and synthesis of 1,5-disubstituted tetrazoles as potent inhibitors of the MDM2-p53 interaction
  26. A Unique Mdm2-Binding Mode of the 3-Pyrrolin-2-one- and 2-Furanone-Based Antagonists of the p53-Mdm2 Interaction
  27. Distinct 3D Architecture and Dynamics of the Human HtrA2(Omi) Protease and Its Mutated Variants
  28. Inhibitors of programmed cell death 1 (PD-1): a patent review (2010-2015)
  29. Visualization of kallikreins in thyroid epithelial and carcinoma cells
  30. Identification of Secreted Exoproteome Fingerprints of Highly-Virulent and Non-Virulent Staphylococcus aureus Strains
  31. Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
  32. Structure of human Programmed cell death 1 ligand 1 (PD-L1) with low molecular mass inhibitor
  33. Structural basis for small molecule targeting of the programmed death ligand 1 (PD-L1)
  34. The outer-membrane export signal of Porphyromonas gingivalis type IX secretion system (T9SS) is a conserved C-terminal β-sandwich domain
  35. Structure of the Complex of Human Programmed Death 1, PD-1, and Its Ligand PD-L1
  36. PD-1 binding domain from human PD-L1
  37. Structure of the complex of human programmed death-1 (PD-1) and its ligand PD-L1.
  38. Investigation of Serine-Proteinase-Catalyzed Peptide Splicing in Analogues of Sunflower Trypsin Inhibitor 1 (SFTI-1)
  39. Structural Basis of GD2 Ganglioside and Mimetic Peptide Recognition by 14G2a Antibody
  40. The Nucleocapsid Protein of Human Coronavirus NL63
  41. Atomic resolution crystal structure of HV-BBI protease inhibitor from amphibian skin in complex with bovine trypsin
  42. A systematic investigation of the stability of green fluorescent protein fusion proteins
  43. Staphylococcal SplB Serine Protease Utilizes a Novel Molecular Mechanism of Activation
  44. Staphylococcal Proteases Aid in Evasion of the Human Complement System
  45. Development and binding characteristics of phosphonate inhibitors of SplA protease from Staphylococcus aureus
  46. Biochemical and Structural Characterization of SplD Protease from Staphylococcus aureus
  47. A regulatory role for Staphylococcus aureus toxin–antitoxin system PemIKSa
  48. Structural phase transition and related electronic properties in quasi-one-dimensional (NbSe4)10/3I
  49. Insights into eukaryotic Rubisco assembly — Crystal structures of RbcX chaperones from Arabidopsis thaliana
  50. Mdm2 and MdmX inhibitors for the treatment of cancer: a patent review (2011 – present)
  51. Bacterial Proteases in Disease – Role in Intracellular Survival, Evasion of Coagulation/ Fibrinolysis Innate Defenses, Toxicoses and Viral Infections
  52. Bacterial Proteases in Disease – Role in Intracellular Survival, Evasion of Coagulation/ Fibrinolysis Innate Defenses, Toxicoses and Viral Infections
  53. Isolation, biochemical characterization, and cloning of a bacteriocin from the poultry-associated Staphylococcus aureus strain CH-91
  54. Staphylococcal proteases aid evasion of human complement system
  55. Prevalence of genes encoding extracellular proteases inStaphylococcus aureus— important targets triggering immune responsein vivo
  56. The virulence of Staphylococcus aureus correlates with strain genotype in a chicken embryo model but not a nematode model
  57. The development of first Staphylococcus aureus SplB protease inhibitors: Phosphonic analogues of glutamine
  58. On the Mechanism of Action of SJ-172550 in Inhibiting the Interaction of MDM4 and p53
  59. Substrate specificity of Staphylococcus aureus cysteine proteases – Staphopains A, B and C
  60. α1-Antichymotrypsin inactivates staphylococcal cysteine protease in cross-class inhibition
  61. Activation mechanism of thiol protease precursor from broiler chicken specific Staphylococcus aureus strain CH-91
  62. Interaction of regulators Mdm2 and Mdmx with transcription factors p53, p63 and p73
  63. Exfoliative Toxins of Staphylococcus aureus
  64. A novel matrix metalloprotease-like enzyme (karilysin) of the periodontal pathogen Tannerella forsythia ATCC 43037
  65. Structural and functional characterization of SplA, an exclusively specific protease of Staphylococcus aureus
  66. High affinity interaction of the p53 peptide-analogue with human Mdm2 and Mdmx
  67. Elafin is specifically inactivated by RgpB from Porphyromonas gingivalis by distinct proteolytic cleavage
  68. Enzymatic Activity of the Staphylococcus aureus SplB Serine Protease is Induced by Substrates Containing the Sequence Trp-Glu-Leu-Gln
  69. Staphylococcus aureusinfection triggers production of neutralizing, V8 protease-specific antibodies
  70. The human fibrinolytic system is a target for the staphylococcal metalloprotease aureolysin
  71. Staphylococcus aureus-Derived Staphopain B, a Potent Cysteine Protease Activator of Plasma Chemerin
  72. The staphostatin family of cysteine protease inhibitors in the genus Staphylococcus as an example of parallel evolution of protease and inhibitor specificity
  73. Functional and Structural Characterization of Spl Proteases from Staphylococcus aureus
  74. Proteinaceous cysteine protease inhibitors
  75. Letter to the Editor: 1 H, 15 N and 13 C NMR Resonance Assignments of Staphostatin A, a Specific Staphylococcus Aureus Cysteine Proteinase Inhibitor
  76. Characterisation of a highly specific, endogenous inhibitor of cysteine protease from Staphylococcus epidermidis, a new member of the staphostatin family
  77. A Novel Class of Cysteine Protease Inhibitors:  Solution Structure of Staphostatin A fromStaphylococcus aureus†
  78. Extracellular Proteases of Staphylococcus spp.
  79. Molecular Cloning and Biochemical Characterisation of Proteases from Staphylococcus epidermidis