Literature DB >> 10806363

The novel G-protein coupled receptor SALPR shares sequence similarity with somatostatin and angiotensin receptors.

M Matsumoto1, M Kamohara, T Sugimoto, K Hidaka, J Takasaki, T Saito, M Okada, T Yamaguchi, K Furuichi.   

Abstract

A cDNA encoding a novel G-protein coupled receptor (GPCR) was isolated from a human cerebral cortex cDNA library by low stringency hybridization screening. This putative seven-transmembrane domain receptor of 469 amino acids was designated SALPR (Somatostatin- and Angiotensin- Like Peptide Receptor). SALPR shares the highest amount of amino acid similarity with the somatostatin (35% with SSTR5) and angiotensin receptors (31% with AT1). Reverse transcription-polymerase chain reaction (RT-PCR) analysis revealed that the SALPR mRNA is predominantly expressed in human brain regions, particularly the substantia nigra and pituitary, although the mRNA can also be detected in the peripheral tissues, albeit at low levels. Chromosomal mapping by radiation hybrid analysis localized the human SALPR gene to the chromosome 5p15.1-5p14. Transient expression of SALPR in COS-1 cells did not produce any binding sites for somatostatin or angiotensin II, indicating the necessity for further study to discover its ligand and physiological significance.

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Year:  2000        PMID: 10806363     DOI: 10.1016/s0378-1119(00)00123-2

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  19 in total

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Review 3.  Relaxin family peptide receptors--former orphans reunite with their parent ligands to activate multiple signalling pathways.

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4.  The Concise Guide to PHARMACOLOGY 2013/14: G protein-coupled receptors.

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5.  Distinct but overlapping binding sites of agonist and antagonist at the relaxin family peptide 3 (RXFP3) receptor.

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Review 6.  Distribution, physiology and pharmacology of relaxin-3/RXFP3 systems in brain.

Authors:  Sherie Ma; Craig M Smith; Anna Blasiak; Andrew L Gundlach
Journal:  Br J Pharmacol       Date:  2016-12-04       Impact factor: 8.739

Review 7.  International Union of Basic and Clinical Pharmacology. XCV. Recent advances in the understanding of the pharmacology and biological roles of relaxin family peptide receptors 1-4, the receptors for relaxin family peptides.

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8.  Discovery and functional characterization of a novel small molecule inhibitor of the intracellular phosphatase, SHIP2.

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9.  Identification and characterisation of GPR100 as a novel human G-protein-coupled bradykinin receptor.

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Journal:  Br J Pharmacol       Date:  2003-10-06       Impact factor: 8.739

10.  In vitro pharmacological characterization of RXFP3 allosterism: an example of probe dependency.

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