The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY
Abstract The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjun...
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Published in | Nucleic acids research Vol. 46; no. D1; pp. D1091 - D1106 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
04.01.2018
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Subjects | |
Online Access | Get full text |
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Abstract | Abstract
The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org). This has been 'forked' from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions. |
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AbstractList | The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org). This has been 'forked' from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions. Abstract The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org). This has been 'forked' from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions. The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org). This has been 'forked' from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions.The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org). This has been 'forked' from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions. The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org ) and its precursor IUPHAR-DB, have captured expert-curated interactions between targets and ligands from selected papers in pharmacology and drug discovery since 2003. This resource continues to be developed in conjunction with the International Union of Basic and Clinical Pharmacology (IUPHAR) and the British Pharmacological Society (BPS). As previously described, our unique model of content selection and quality control is based on 96 target-class subcommittees comprising 512 scientists collaborating with in-house curators. This update describes content expansion, new features and interoperability improvements introduced in the 10 releases since August 2015. Our relationship matrix now describes ∼9000 ligands, ∼15 000 binding constants, ∼6000 papers and ∼1700 human proteins. As an important addition, we also introduce our newly funded project for the Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb, www.guidetoimmunopharmacology.org ). This has been ‘forked’ from the well-established GtoPdb data model and expanded into new types of data related to the immune system and inflammatory processes. This includes new ligands, targets, pathways, cell types and diseases for which we are recruiting new IUPHAR expert committees. Designed as an immunopharmacological gateway, it also has an emphasis on potential therapeutic interventions. |
Author | Sharman, Joanna L Pawson, Adam J Davenport, Anthony P Doerig, Christian Fabbro, Doriano Bruce, Liam Alexander, Stephen P H Southan, Chris Spedding, Michael Faccenda, Elena Bryant, Clare Harding, Simon D Davies, Jamie A Gray, Alasdair J G Anderton, Stephen Levi-Schaffer, Francesca Ireland, Sam |
AuthorAffiliation | School of Mathematical and Computer Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge CB2 0QQ, UK Spedding Research Solutions SAS, Le Vésinet 78110, France School of Life Sciences, University of Nottingham Medical School, Nottingham NG7 2UH, UK MRC Centre for inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, UK Pharmacology and Experimental Therapeutics Unit, School of Pharmacy, Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem 9112102, Israel Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK Department of Microbiology, Monash University, Clayton 3800, Australia Department of Structural & Molecular Biology, University College London, London WC1E 6BT, UK Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK PIQUR Therapeutics, Basel 4057, Switzerland |
AuthorAffiliation_xml | – name: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK – name: Spedding Research Solutions SAS, Le Vésinet 78110, France – name: School of Mathematical and Computer Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK – name: MRC Centre for inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, UK – name: Department of Structural & Molecular Biology, University College London, London WC1E 6BT, UK – name: Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK – name: Pharmacology and Experimental Therapeutics Unit, School of Pharmacy, Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem 9112102, Israel – name: School of Life Sciences, University of Nottingham Medical School, Nottingham NG7 2UH, UK – name: PIQUR Therapeutics, Basel 4057, Switzerland – name: Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge CB2 0QQ, UK – name: Department of Microbiology, Monash University, Clayton 3800, Australia |
Author_xml | – sequence: 1 givenname: Simon D orcidid: 0000-0002-9262-8318 surname: Harding fullname: Harding, Simon D organization: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK – sequence: 2 givenname: Joanna L surname: Sharman fullname: Sharman, Joanna L organization: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK – sequence: 3 givenname: Elena surname: Faccenda fullname: Faccenda, Elena organization: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK – sequence: 4 givenname: Chris surname: Southan fullname: Southan, Chris organization: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK – sequence: 5 givenname: Adam J surname: Pawson fullname: Pawson, Adam J organization: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK – sequence: 6 givenname: Sam surname: Ireland fullname: Ireland, Sam organization: Department of Structural & Molecular Biology, University College London, London WC1E 6BT, UK – sequence: 7 givenname: Alasdair J G surname: Gray fullname: Gray, Alasdair J G organization: School of Mathematical and Computer Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK – sequence: 8 givenname: Liam surname: Bruce fullname: Bruce, Liam organization: School of Mathematical and Computer Sciences, Heriot-Watt University, Edinburgh EH14 4AS, UK – sequence: 9 givenname: Stephen P H surname: Alexander fullname: Alexander, Stephen P H organization: School of Life Sciences, University of Nottingham Medical School, Nottingham NG7 2UH, UK – sequence: 10 givenname: Stephen surname: Anderton fullname: Anderton, Stephen organization: MRC Centre for inflammation Research, University of Edinburgh, Edinburgh EH16 4TJ, UK – sequence: 11 givenname: Clare surname: Bryant fullname: Bryant, Clare organization: Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, UK – sequence: 12 givenname: Anthony P surname: Davenport fullname: Davenport, Anthony P organization: Experimental Medicine and Immunotherapeutics, University of Cambridge, Cambridge CB2 0QQ, UK – sequence: 13 givenname: Christian surname: Doerig fullname: Doerig, Christian organization: Department of Microbiology, Monash University, Clayton 3800, Australia – sequence: 14 givenname: Doriano surname: Fabbro fullname: Fabbro, Doriano organization: PIQUR Therapeutics, Basel 4057, Switzerland – sequence: 15 givenname: Francesca surname: Levi-Schaffer fullname: Levi-Schaffer, Francesca organization: Pharmacology and Experimental Therapeutics Unit, School of Pharmacy, Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem 9112102, Israel – sequence: 16 givenname: Michael surname: Spedding fullname: Spedding, Michael organization: Spedding Research Solutions SAS, Le Vésinet 78110, France – sequence: 17 givenname: Jamie A surname: Davies fullname: Davies, Jamie A email: jamie.davies@ed.ac.uk organization: Deanery of Biomedical Sciences, University of Edinburgh, Edinburgh EH8 9XD, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29149325$$D View this record in MEDLINE/PubMed |
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The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions... The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org) and its precursor IUPHAR-DB, have captured expert-curated interactions between... The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb, www.guidetopharmacology.org ) and its precursor IUPHAR-DB, have captured expert-curated interactions between... |
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Title | The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY |
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