G protein-coupled receptor

large protein family of receptors that detect molecules outside the cell and activate internal signal transduction pathways and cellular responses

DBpedia resource is: http://dbpedia.org/resource/G_protein-coupled_receptor

Abstract is: G protein-coupled receptors (GPCRs), also known as seven-(pass)-transmembrane domain receptors, 7TM receptors, heptahelical receptors, serpentine receptors, and G protein-linked receptors (GPLR), form a large group of evolutionarily-related proteins that are cell surface receptors that detect molecules outside the cell and activate cellular responses. Coupling with G proteins, they are called seven-transmembrane receptors because they pass through the cell membrane seven times. Ligands can bind either to extracellular N-terminus and loops (e.g. glutamate receptors) or to the binding site within transmembrane helices (Rhodopsin-like family). They are all activated by agonists although a spontaneous auto-activation of an empty receptor can also be observed. G protein-coupled receptors are found only in eukaryotes, including yeast, choanoflagellates, and animals. The ligands that bind and activate these receptors include light-sensitive compounds, odors, pheromones, hormones, and neurotransmitters, and vary in size from small molecules to peptides to large proteins. G protein-coupled receptors are involved in many diseases. There are two principal signal transduction pathways involving the G protein-coupled receptors: * the cAMP signal pathway and * the phosphatidylinositol signal pathway. When a ligand binds to the GPCR it causes a conformational change in the GPCR, which allows it to act as a guanine nucleotide exchange factor (GEF). The GPCR can then activate an associated G protein by exchanging the GDP bound to the G protein for a GTP. The G protein's α subunit, together with the bound GTP, can then dissociate from the β and γ subunits to further affect intracellular signaling proteins or target functional proteins directly depending on the α subunit type (Gαs, Gαi/o, Gαq/11, Gα12/13). GPCRs are an important drug target and approximately 34% of all Food and Drug Administration (FDA) approved drugs target 108 members of this family. The global sales volume for these drugs is estimated to be 180 billion US dollars as of 2018. It is estimated that GPCRs are targets for about 50% of drugs currently on the market, mainly due to their involvement in signaling pathways related to many diseases i.e. mental, metabolic including endocrinological disorders, immunological including viral infections, cardiovascular, inflammatory, senses disorders, and cancer. The long ago discovered association between GPCRs and many endogenous and exogenous substances, resulting in e.g. analgesia, is another dynamically developing field of the pharmaceutical research.

Wikimedia Commons category is G protein-coupled receptors

G protein-coupled receptor is …
instance of (P31):
group or class of transmembrane transport proteinsQ67101749

sublass of (P279):
transporter of unknown biochemical mechanismQ69533762
transmembrane signaling receptorQ106952156
metabotropic receptorQ901988
cell surface receptorQ2476074

External links are
P2581BabelNet ID00462444n
00462444n
P10565Encyclopedia of China (Third Edition) ID76509
P1417Encyclopædia Britannica Online IDscience/G-protein-coupled-receptor
P646Freebase ID/m/03c91
P3827JSTOR topic ID (archived)g-protein-coupled-receptors
P8408KBpedia IDGProteinCoupledReceptor
P486MeSH descriptor IDD043562
P672MeSH tree codeD12.776.543.750.695
P6366Microsoft Academic ID135285700
P10283OpenAlex IDC135285700
P7260Transporter Classification Database ID9.A.14
P2892UMLS CUIC0682972

P680molecular functionG protein-coupled receptor activityQ14859545
P910topic's main categoryCategory:G protein-coupled receptorsQ8479306
P1424topic's main templateTemplate:G protein-coupled receptorsQ11110390