Cholecystokinin A receptor: Difference between revisions
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| summary_text = This gene encodes a G-protein coupled receptor that binds |
| summary_text = This gene encodes a G-protein coupled receptor that binds sulfated members of the cholecystokinin (CCK) family of peptide hormones. This receptor is a major physiologic mediator of pancreatic enzyme secretion and smooth muscle contraction of the gallbladder and stomach. In the central and peripheral nervous system this receptor regulates satiety and the release of beta-endorphin and dopamine.<ref name="entrez">{{cite web | title = Entrez Gene: CCKAR cholecystokinin A receptor| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=886| accessdate = }}</ref> |
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Revision as of 21:31, 23 January 2016
Cholecystokinin A receptor, N-terminal domain | |||||||||
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Identifiers | |||||||||
Symbol | CholecysA-Rec_N | ||||||||
Pfam | PF09193 | ||||||||
InterPro | IPR015276 | ||||||||
SCOP2 | 1d6g / SCOPe / SUPFAM | ||||||||
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The Cholecystokinin A receptor is a human protein, also known as CCKAR or CCK1, with CCK1 now being the IUPHAR-recommended name.
The extracellular, N-terminal, domain of this protein adopts a tertiary structure consisting of a few helical turns and a disulfide-cross linked loop. It is required for interaction of the cholecystokinin A receptor with its corresponding hormonal ligand.[1]
Selective Ligands
Agonists
- Cholecystokinin
- Gastrin
- CCK-4
- SR-146,131
- A-71623 - modified tetrapeptide, potent and selective CCKA agonist, IC50 3.7nM, 1200x selectivity over CCKB, CAS# 130408-77-4
Antagonists
- Proglumide
- Lorglumide
- Devazepide
- Dexloxiglumide
- Asperlicin
- SR-27897
- IQM-95333
- JNJ-17156516
See also
References
- ^ Pellegrini M, Mierke DF (November 1999). "Molecular complex of cholecystokinin-8 and N-terminus of the cholecystokinin A receptor by NMR spectroscopy". Biochemistry. 38 (45): 14775–83. doi:10.1021/bi991272l. PMID 10555959.
External links
- "Cholecystokinin Receptors: CCK1". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.
Further reading
This article incorporates text from the United States National Library of Medicine, which is in the public domain.