All Stories

  1. A rational roadmap for SARS‐CoV‐2/COVID‐19 pharmacotherapeutic research and development. IUPHAR Review 29
  2. Opening up connectivity between documents, structures and bioactivity
  3. Déjà vu: Stimulating Open Drug Discovery for SARS-CoV-2
  4. Hydrolases (version 2019.5) in the IUPHAR/BPS Guide to Pharmacology Database
  5. Hydrolases (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
  6. A new guide to immunopharmacology
  7. Challenges of Connecting Chemistry to Pharmacology: Perspectives from Curating the IUPHAR/BPS Guide to PHARMACOLOGY
  8. SynPharm - a new tool to help Synthetic Biologists create proteins which respond to existing drugs
  9. Accessing Expert-Curated Pharmacological Data in the IUPHAR/BPS Guide to PHARMACOLOGY
  10. Caveat Usor: Assessing Differences between Major Chemistry Databases
  11. An open-access tool for designing drug control into engineered proteins
  12. Challenges of Connecting Chemistry to Pharmacology: Perspectives from Curating the IUPHAR/BPS Guide to PHARMACOLOGY
  13. Can we devise new therapies by combining databases of protein interactions and of drug targets?
  14. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Catalytic receptors
  15. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Other ion channels
  16. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Enzymes
  17. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Transporters
  18. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: G protein-coupled receptors
  19. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Ligand-gated ion channels
  20. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Nuclear hormone receptors
  21. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Overview
  22. THE CONCISE GUIDE TO PHARMACOLOGY 2017/18: Voltage-gated ion channels
  23. Counting human proteins
  24. OUP accepted manuscript
  25. Selected GPCR resources
  26. Illustrating and homology modeling the proteins of the Zika virus
  27. The endothelin hormones, structure and function
  28. Modeling the proteins in the Zika virus
  29. The Concise Guide to PHARMACOLOGY 2015/16: Catalytic receptors
  30. A focus on the enzymes for which there is pharmacological or therapeutic interest
  31. The Concise Guide to PHARMACOLOGY 2015/16: G protein-coupled receptors
  32. The Concise Guide to PHARMACOLOGY 2015/16: Ligand-gated ion channels
  33. The Concise Guide to PHARMACOLOGY 2015/16: Nuclear hormone receptors
  34. The Concise Guide to PHARMACOLOGY 2015/16: Other ion channels
  35. The Concise Guide to PHARMACOLOGY 2015/16: Transporters
  36. The Concise Guide to PHARMACOLOGY 2015/16: Voltage-gated ion channels
  37. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands
  38. Addressing the next viral outbreak
  39. Expanding opportunities for mining bioactive chemistry from patents
  40. How do we fight the next pathogen we discover?
  41. Associated challenges with the divergent expansions of public and commercial sources of molecules
  42. Comparing the Chemical Structure and Protein Content of ChEMBL, DrugBank, Human Metabolome Database and the Therapeutic Target Database
  43. The IUPHAR/BPS Guide to PHARMACOLOGY: an expert-driven knowledgebase of drug targets and their ligands
  44. Tracking 20 Years of Compound-to-Target Output from Literature and Patents
  45. Extracting and connecting chemical structures from text sources using chemicalize.org
  46. BACE2 as a new diabetes target: a patent review (2010 – 2012)
  47. InChI in the wild: an assessment of InChIKey searching in Google
  48. Challenges associated with obtaining chemical structures of repurposing candidates from an online DB
  49. A tale of two drug targets: the evolutionary history of BACE1 and BACE2
  50. Shouldn't enantiomeric purity be included in the 'minimum information about a bioactive entity? Response from the MIABE group
  51. SARConnect: A Tool to Interrogate the Connectivity Between Proteins, Chemical Structures and Activity Data
  52. Mapping Between Databases of Compounds and Protein Targets
  53. Making every SAR point count: the development of Chemistry Connect for the large-scale integration of structure and bioactivity data
  54. Minimum information about a bioactive entity (MIABE)
  55. Analysis of in vitrobioactivity data extracted from drug discovery literature and patents: Ranking 1654 human protein targets by assayed compounds and molecular scaffolds
  56. Towards BioDBcore: a community-defined information specification for biological databases
  57. Towards BioDBcore: a community-defined information specification for biological databases
  58. The Cinderella of Biological Data Integration: Addressing Some of the Challenges of Entity and Relationship Mining from Patent Sources
  59. Quantitative assessment of the expanding complementarity between public and commercial databases of bioactive compounds
  60. The Yoyo Has Stopped: Reviewing the Evidence for a Low Basal Human Protein Number
  61. Thrombin-induced fibrinopeptide release from a fibrinogen variant (fibrinogen Sydney I) with an Aα Arg-16 → His substitution
  62. Proteases: Evolution
  63. Complementarity Between Public and Commercial Databases: New Opportunities in Medicinal Chemistry Informatics
  64. Exploiting new genome data and Internet resources for the phylogenetic analysis of proteases, substrates and inhibitors
  65. Finding, Delineating and Analysing Genes
  66. Proteases: Evolution
  67. Has the yo-yo stopped? An assessment of human protein-coding gene number
  68. Splice variants: A homology modeling approach
  69. The HtrA Family of Proteases
  70. The characterisation of novel secreted Ly-6 proteins from rat urine by the combined use of two-dimensional gel electrophoresis, microbore high performance liquid chromatography and expressed sequence tag data
  71. Identification, Genomic Organization, and mRNA Expression of LACTB, Encoding a Serine β-Lactamase-like Protein with an Amino-terminal Transmembrane Domain
  72. A genomic perspective on human proteases as drug targets
  73. A genomic perspective on human proteases
  74. Website Review: InterPro (The Integrated Resource of Protein Domains and Functional Sites). http://www.ebi.ac.uk/interpro/
  75. ASP1 (BACE2) Cleaves the Amyloid Precursor Protein at the β-Secretase Site
  76. Characterization of human HtrA2, a novel serine protease involved in the mammalian cellular stress response
  77. THE VERTEBRATE HTRA SERINE PROTEASE FAMILY; A NEW EXAMPLE OF HORIZONTAL GENE TRANSFER
  78. Sequencing, tissue distribution and chromosomal assignment of a novel ubiquitin-specific protease USP23
  79. Assessing the protease and protease inhibitor content of the human genome
  80. The Impact of Genomics on Drug Discovery
  81. InterPro (The Integrated Resource of Protein Domains and Functional Sites)
  82. Identification of a Novel Aspartic Protease (Asp 2) as β-Secretase
  83. Disposable Microbore High-Pressure Liquid Chromatography Columns for Protein and Peptide Separations
  84. Synergistic scale-down of three protein micropreparation techniques
  85. CHROMATOGRAPHIC CARBON AS AN INERT SAMPLE ADSORBENT FOR PROTEIN SEQUENCING
  86. Analytical and micropreparative capillary electrophoresis of the peptides from calcitonin
  87. Separation by capillary electrophoresis followed by dynamic elution
  88. Bovine dopamine .beta.-hydroxylase, primary structure determined by cDNA cloning and amino acid sequencing
  89. Inactivation of dopamine β-hydroxylase by p-cresol: Evidence for a second, minor site of covalent modification at tyrosine 357
  90. Purification to apparent homogeneity and partial amino acid sequence of rat liver O 6 -alkylguanine-DNA-alkyltransferase
  91. Sequence similarity between dopamine β‐hydroxylase and peptide α‐amidating enzyme: Evidence for a conserved catalytic domain
  92. Inactivation of dopamine .beta.-hydroxylase by .beta.-ethynyltyramine: kinetic characterization and covalent modification of an active site peptide
  93. THE USE OF GLASS CAPILLARY TUBES AS DISPOSABLE MICROBORE COLUMNS FOR RP-HPLC OF PROTEINS AND PEPTIDES
  94. Inactivation of dopamine .beta.-hydroxylase by p-cresol: isolation and characterization of covalently modified active site peptides
  95. The nitroreductase enzyme in walker cells that activates 5-(aziridin-1-yl)-2,4-dinitrobenzamide (CB 1954) to 5-(aziridin-1-YL)-4-hydroxylamino-2-nitrobenzamide is a form of NAD(P)H dehydrogenase (quinone) (EC 1.6.99.2)
  96. Use of sep-pak cartridges for on-line preparative high-performance liquid chromatography
  97. Amino acid sequence of β‐galactoside‐binding bovine heart lectin
  98. Direct analysis of plasma fibrinogen‐derived fibrinopeptides by high‐performance liquid chromatography: investigation of nine congenital fibrinogen abnormalities
  99. Direct analysis of plasma fibrinogen-derived fibrinopeptides by high-performance liquid chromatography
  100. COVALENT STRUCTURE OF FIBRINOGEN
  101. Fibrinogen Manchester: identification of an abnormal fibrinopeptide A with a C-terminal arginine→histidine substitution
  102. Delayed release of an abnormal fibrinopeptide A from fibrinogen Manchester: effect of the Aα 16 Arg → His substitution upon fibrin monomer polymerization and the immunological crossreactivity of the peptide
  103. The ELIXIR Database Provider Survey
  104. Finding, Delineating and Analysing Genes
  105. Internet Resources for the Geneticist
  106. A Bioinformatics Perspective on Genetics in Drug Discovery and Development