International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G Protein–Coupled Receptors
Copyright policy )International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G Protein–Coupled Receptors
The Adhesion family forms a large branch of the pharmacologically important superfamily of G protein-coupled receptors (GPCRs). As Adhesion GPCRs increasingly receive attention from a wide spectrum of biomedical fields, the Adhesion GPCR Consortium, together with the International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug Classification, proposes a unified nomenclature for Adhesion GPCRs. The new names have ADGR as common dominator followed by a letter and a number to denote each subfamily and subtype, respectively. The new names, with old and alternative names within parentheses, are: ADGRA1 (GPR123), ADGRA2 (GPR124), ADGRA3 (GPR125), ADGRB1 (BAI1), ADGRB2 (BAI2), ADGRB3 (BAI3), ADGRC1 (CELSR1), ADGRC2 (CELSR2), ADGRC3 (CELSR3), ADGRD1 (GPR133), ADGRD2 (GPR144), ADGRE1 (EMR1, F4/80), ADGRE2 (EMR2), ADGRE3 (EMR3), ADGRE4 (EMR4), ADGRE5 (CD97), ADGRF1 (GPR110), ADGRF2 (GPR111), ADGRF3 (GPR113), ADGRF4 (GPR115), ADGRF5 (GPR116, Ig-Hepta), ADGRG1 (GPR56), ADGRG2 (GPR64, HE6), ADGRG3 (GPR97), ADGRG4 (GPR112), ADGRG5 (GPR114), ADGRG6 (GPR126), ADGRG7 (GPR128), ADGRL1 (latrophilin-1, CIRL-1, CL1), ADGRL2 (latrophilin-2, CIRL-2, CL2), ADGRL3 (latrophilin-3, CIRL-3, CL3), ADGRL4 (ELTD1, ETL), and ADGRV1 (VLGR1, GPR98). This review covers all major biologic aspects of Adhesion GPCRs, including evolutionary origins, interaction partners, signaling, expression, physiologic functions, and therapeutic potential.
- King's College London United Kingdom
- Stanford University United States
- Washington University in St. Louis United States
- Emory University United States
- University of Amsterdam Netherlands
Models, Molecular, Pharmacology, Societies, Scientific, Cell Membrane, 610, International Agencies, Ligands, QP, Second Messenger Systems, Receptors, G-Protein-Coupled, Cell Movement, Terminology as Topic, Pharmacology, Clinical, Cell Adhesion, Cyclic AMP, Animals, Humans, Protein Isoforms, QP517, Cell Adhesion Molecules, Signal Transduction
Models, Molecular, Pharmacology, Societies, Scientific, Cell Membrane, 610, International Agencies, Ligands, QP, Second Messenger Systems, Receptors, G-Protein-Coupled, Cell Movement, Terminology as Topic, Pharmacology, Clinical, Cell Adhesion, Cyclic AMP, Animals, Humans, Protein Isoforms, QP517, Cell Adhesion Molecules, Signal Transduction
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