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GtoImmuPdb Portal
Aims
●
A unique access-point to
immunological data in
GtoPdb
●
An expert-curated
database containing
immunological
information
●
Develop new pages and
extend search mechanism
for immunological data
●
Assist in the identification
of novel therapeutic
targets
●
Assist in identifying
small-molecules for
experimental
investigation
S. D. Harding1
, E. Faccenda1
, S. Ireland1
, A. J. Pawson1
, J. L. Sharman1
, C. Southan1
, S. P. Alexander2
,
S. Anderton3
, C. Bryant4
, A. P. Davenport5
, C. Doerig6
, D. Fabbro7
, F. Levi-Schaffer8
, M. Spedding9
, J. A. Davies1
1Centre for Integrative Physiology, School of Biomedical Sciences, University of Edinburgh, Edinburgh, UNITED KINGDOM, 2Life Sciences, University of Nottingham, Nottingham, UNITED KINGDOM,3MRC Centre for Inflammation Research, QMRI, University
of Edinburgh, Edinburgh, UNITED KINGDOM, 4
Veterinary Medicine, University of Cambridge, Cambridge, UNITED KINGDOM,5
Clinical Pharmacology Unit, University of Cambridge, Cambridge, UNITED KINGDOM, 6
Department of Microbiology, Monash
University, Clayton, AUSTRALIA, 7PIQUR Therapeutics AG, Basel, SWITZERLAND, 8School of Pharmacy, Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem, ISRAEL, 9Spedding Research Solutions SARL, Le Vesinet, FRANCE.
Introduction
Background
Immune/inflammatory/infection responses and disorders are a major focus of
pharmacological R&D. Chronic diseases, aspects of ageing and progress of infection all
have, or depend strongly on, an immune, or inflammatory, component. Being able to
modulate these more effectively with better drugs would be immensely valuable.
Development of these drugs will benefit from improved data exchange between the
immunology expert and pharmacology expert communities.
What is the Guide to IMMUNOPHARMACOLOGY
Our Wellcome Trust-funded project to produce the IUPHAR Guide to
IMMUNOPHARMACOLOGY (GtoImmuPdb) addresses this need by providing a new
portal to the existing IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb), that is both
'immunologist-friendly' for pharmacological information and 'pharmacologist-friendly'
for accessing immunological agents and targets. GtoImmuPdb will be a freely-available,
regularly updated and richly annotated resource. Curated by expert NC-IUPHAR*
sub-committees, including additional contributors with expertise in immunity,
inflammation and kinase biology.
GtoImmuPdb Data
The GtoP database has been enriched by tagging targets & ligands of
immunological relevance and by linking these to immunological processes, cell
types and relevant diseases.
Beta-version v2.0 available at:
www.guidetoimmunopharmacology.org
The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb) is an open access
resource providing overviews of key properties, background reading and
selective ligands of a wide range of biological targets.
The searchable database provides
quantitative information on drug
targets and the prescription medicines
and experimental drugs that act on
them. For ligands, data on approved
status, clinical use and mechanism of
action are included.
References
* International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug
Classification
1. Harding SD, et al. (2018) The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: Updates and expansion to
encompass the new Guide to IMMUNOPHARMACOLOGY. Nucl. Acids Res. PMID: 29149325
2. Cell Ontology, http://obofoundry.org/ontology/cl.html ontology.org
3. Gene Ontology Consortium, http://geneontology.org
Human targets in GtoPdb, 2017.5 release
Ligand classes in GtoPdb, 2017.5 release
The 2017.5 release (August 2017)
of the database contains over
15,200 curated interactions across
1,684 human targets and 8,978
ligands. More specifically, the
database contains 1,431 human
targets that have quantitative
interactions to a ligand.
Immuno Process and Cell Type Data
GtoImmuPdb presents a set of top-level immunological process and cell type
categories against which targets in the database can be annotated and which
form the basis of organising, navigating and searching for immunological
process and cell type associations.
Subsets of these ontologies are mapped to each top-level category. This then
forms the basis of searches which will detect any cell type or process
associations annotated with those terms (or their children).
Target detailed view pages
display process and cell
type associations
Including detailed curator
comments and links to
external references
As of 9 Oct 2017 the development GtoImmuPdb held 455 protein targets
and 816 ligands tagged as being of immunological relevance.
GtoImmuPdb uses both
Cell Ontology1
and Gene
Ontology2
terms as
controlled vocabularies
against which to
annotate. Displaying GtoImmuPdb data in detailed view of BTK
Immuno Cell Types
B cells
Dendritic cells
Granulocytes
Innate lymphoid cells
Macrophages & monocytes
Mast cells
Natural killer cells
Other T cells
T cells
Stromal cells
Immuno Processes
Antigen presentation
Barrier integrity
B cell (activation)
Cellular signalling
Chemotaxis & migration
Cytokine production & signalling
Immune regulation
Immune system development
Inflammation
T cell (activation)
Tissue repair
Targets Ligands
Cell types Processes
Disease
Target family pages use a toggle
to switch between GtoPdb &
GtoImmuPdb views
Ligand lists highlight
immuno relevant ligands
with new icons.
Here showing inhibitors
of BTK
IUPHAR Guide to
IMMUNOPHARMACOLOGY

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GtoImmuPdb_2017

  • 1. Thank you to the BSI for supporting this poster: GtoImmuPdb Portal Aims ● A unique access-point to immunological data in GtoPdb ● An expert-curated database containing immunological information ● Develop new pages and extend search mechanism for immunological data ● Assist in the identification of novel therapeutic targets ● Assist in identifying small-molecules for experimental investigation S. D. Harding1 , E. Faccenda1 , S. Ireland1 , A. J. Pawson1 , J. L. Sharman1 , C. Southan1 , S. P. Alexander2 , S. Anderton3 , C. Bryant4 , A. P. Davenport5 , C. Doerig6 , D. Fabbro7 , F. Levi-Schaffer8 , M. Spedding9 , J. A. Davies1 1Centre for Integrative Physiology, School of Biomedical Sciences, University of Edinburgh, Edinburgh, UNITED KINGDOM, 2Life Sciences, University of Nottingham, Nottingham, UNITED KINGDOM,3MRC Centre for Inflammation Research, QMRI, University of Edinburgh, Edinburgh, UNITED KINGDOM, 4 Veterinary Medicine, University of Cambridge, Cambridge, UNITED KINGDOM,5 Clinical Pharmacology Unit, University of Cambridge, Cambridge, UNITED KINGDOM, 6 Department of Microbiology, Monash University, Clayton, AUSTRALIA, 7PIQUR Therapeutics AG, Basel, SWITZERLAND, 8School of Pharmacy, Institute for Drug Research, Hebrew University of Jerusalem, Jerusalem, ISRAEL, 9Spedding Research Solutions SARL, Le Vesinet, FRANCE. Introduction Background Immune/inflammatory/infection responses and disorders are a major focus of pharmacological R&D. Chronic diseases, aspects of ageing and progress of infection all have, or depend strongly on, an immune, or inflammatory, component. Being able to modulate these more effectively with better drugs would be immensely valuable. Development of these drugs will benefit from improved data exchange between the immunology expert and pharmacology expert communities. What is the Guide to IMMUNOPHARMACOLOGY Our Wellcome Trust-funded project to produce the IUPHAR Guide to IMMUNOPHARMACOLOGY (GtoImmuPdb) addresses this need by providing a new portal to the existing IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb), that is both 'immunologist-friendly' for pharmacological information and 'pharmacologist-friendly' for accessing immunological agents and targets. GtoImmuPdb will be a freely-available, regularly updated and richly annotated resource. Curated by expert NC-IUPHAR* sub-committees, including additional contributors with expertise in immunity, inflammation and kinase biology. GtoImmuPdb Data The GtoP database has been enriched by tagging targets & ligands of immunological relevance and by linking these to immunological processes, cell types and relevant diseases. Beta-version v2.0 available at: www.guidetoimmunopharmacology.org The IUPHAR/BPS Guide to PHARMACOLOGY (GtoPdb) is an open access resource providing overviews of key properties, background reading and selective ligands of a wide range of biological targets. The searchable database provides quantitative information on drug targets and the prescription medicines and experimental drugs that act on them. For ligands, data on approved status, clinical use and mechanism of action are included. References * International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug Classification 1. Harding SD, et al. (2018) The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: Updates and expansion to encompass the new Guide to IMMUNOPHARMACOLOGY. Nucl. Acids Res. PMID: 29149325 2. Cell Ontology, http://obofoundry.org/ontology/cl.html ontology.org 3. Gene Ontology Consortium, http://geneontology.org Human targets in GtoPdb, 2017.5 release Ligand classes in GtoPdb, 2017.5 release The 2017.5 release (August 2017) of the database contains over 15,200 curated interactions across 1,684 human targets and 8,978 ligands. More specifically, the database contains 1,431 human targets that have quantitative interactions to a ligand. Immuno Process and Cell Type Data GtoImmuPdb presents a set of top-level immunological process and cell type categories against which targets in the database can be annotated and which form the basis of organising, navigating and searching for immunological process and cell type associations. Subsets of these ontologies are mapped to each top-level category. This then forms the basis of searches which will detect any cell type or process associations annotated with those terms (or their children). Target detailed view pages display process and cell type associations Including detailed curator comments and links to external references As of 9 Oct 2017 the development GtoImmuPdb held 455 protein targets and 816 ligands tagged as being of immunological relevance. GtoImmuPdb uses both Cell Ontology1 and Gene Ontology2 terms as controlled vocabularies against which to annotate. Displaying GtoImmuPdb data in detailed view of BTK Immuno Cell Types B cells Dendritic cells Granulocytes Innate lymphoid cells Macrophages & monocytes Mast cells Natural killer cells Other T cells T cells Stromal cells Immuno Processes Antigen presentation Barrier integrity B cell (activation) Cellular signalling Chemotaxis & migration Cytokine production & signalling Immune regulation Immune system development Inflammation T cell (activation) Tissue repair Targets Ligands Cell types Processes Disease Target family pages use a toggle to switch between GtoPdb & GtoImmuPdb views Ligand lists highlight immuno relevant ligands with new icons. Here showing inhibitors of BTK IUPHAR Guide to IMMUNOPHARMACOLOGY