GPCR/G protein


All GPCRs share a common seven trans-membrane structure. GPCRs are associated with heterotrimeric G-proteins which are GTP-binding proteins made of alpha, beta, and gamma subunits. When a ligand binds to GPCR, it activates the attached G-protein, the GDP is replaced with GTP. The activated G-protein then dissociates into an alpha and a beta-gamma complex which activates downstream signaling pathways. These intracellular signaling pathways include cAMP/PKA, calcium/NFAT, phospholipase C, protein tyrosine kinases, MAP kinases, PI-3-kinase, nitric oxide/cGMP, Rho, and JAK/STAT.
GPCRs are one of the most important therapeutic targets for various diseases, over 30% of all modern medicinal drugs target this family. Aberrant GPCR functions are involved in pathological conditions such as neurological, immunological and hormonal disorders. A large number of GPCRs have been identified, but whose ligands are not known, are classified as orphan receptors.
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N1722 SinomenineSummary: Natural anti-inflammatory agent for treatment of rheumatism and arthritis -
N1825 OstholeTarget: Histamine H1 ReceptorsSummary: Antitumor reagent -
N2537 Peimisine -
N2468 Isocorynoxeine -
N2337 Gramine1 Citation -
N2083 Ligustroflavone -
N2585 Pectolinarin -
N2091 (+)- Corydaline -
N2538 Baohuoside I -
N2298 Xanthotoxol

