Literature DB >> 16491103

Common ligands of G-protein-coupled receptors and arginine-utilizing enzymes.

András Hrabák1.   

Abstract

A new family of G-protein-coupled receptors (GPRC6A) has recently been described and characterized with unknown physiological role. Three isoforms of GPRC6A are expressed from the same gene by alternative splicing. Agonists for GPRC6A are basic amino acids, particularly the analogues and derivatives of L-arginine and L-ornithine. These compounds are known ligands of nitric oxide synthase and arginase isoenzymes, but amino-acid sequences of these enzymes have not shown significant homologies. Various hypotheses for physiological roles of these receptors have been proposed but not yet substantiated. In order to define the most potent agonists, and elucidate further the biological significance of the receptor family, a detailed ligand-based quantitative structure-activity relationship study may be helpful.

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Year:  2006        PMID: 16491103      PMCID: PMC1760713          DOI: 10.1038/sj.bjp.0706683

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  18 in total

Review 1.  Evolution, structure, and activation mechanism of family 3/C G-protein-coupled receptors.

Authors:  Jean-Philippe Pin; Thierry Galvez; Laurent Prézeau
Journal:  Pharmacol Ther       Date:  2003-06       Impact factor: 12.310

2.  Computer-aided comparison of the inhibition of arginase and nitric oxide synthase in macrophages by amino acids not related to arginine.

Authors:  A Hrabák; T Bajor; A Temesi
Journal:  Comp Biochem Physiol B Biochem Mol Biol       Date:  1996-02       Impact factor: 2.231

3.  The inhibitory effect of nitrite, a stable product of nitric oxide (NO) formation, on arginase.

Authors:  A Hrabák; T Bajor; A Temesi; G Mészáros
Journal:  FEBS Lett       Date:  1996-07-22       Impact factor: 4.124

4.  Inhibition of rat liver arginase by an intermediate in NO biosynthesis, NG-hydroxy-L-arginine: implications for the regulation of nitric oxide biosynthesis by arginase.

Authors:  F Daghigh; J M Fukuto; D E Ash
Journal:  Biochem Biophys Res Commun       Date:  1994-07-15       Impact factor: 3.575

5.  Molecular similarities in the ligand binding pockets of an odorant receptor and the metabotropic glutamate receptors.

Authors:  Donghui Kuang; Yi Yao; Minghua Wang; N Pattabiraman; Lakshmi P Kotra; David R Hampson
Journal:  J Biol Chem       Date:  2003-08-11       Impact factor: 5.157

6.  Molecular cloning, expression, and sequence analysis of GPRC6A, a novel family C G-protein-coupled receptor.

Authors:  Petrine Wellendorph; Hans Bräuner-Osborne
Journal:  Gene       Date:  2004-06-23       Impact factor: 3.688

7.  Comparison of substrate and inhibitor specificity of arginase and nitric oxide (NO) synthase for arginine analogues and related compounds in murine and rat macrophages.

Authors:  A Hrabák; T Bajor; A Temesi
Journal:  Biochem Biophys Res Commun       Date:  1994-01-14       Impact factor: 3.575

8.  Known regulators of nitric oxide synthase and arginase are agonists at the human G-protein-coupled receptor GPRC6A.

Authors:  Bolette Christiansen; Petrine Wellendorph; Hans Bräuner-Osborne
Journal:  Br J Pharmacol       Date:  2006-04       Impact factor: 8.739

9.  Cloning and characterization of an extracellular Ca(2+)-sensing receptor from bovine parathyroid.

Authors:  E M Brown; G Gamba; D Riccardi; M Lombardi; R Butters; O Kifor; A Sun; M A Hediger; J Lytton; S C Hebert
Journal:  Nature       Date:  1993-12-09       Impact factor: 49.962

10.  Isothioureas: potent inhibitors of nitric oxide synthases with variable isoform selectivity.

Authors:  G J Southan; C Szabó; C Thiemermann
Journal:  Br J Pharmacol       Date:  1995-01       Impact factor: 8.739

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  1 in total

Review 1.  Molecular basis for amino acid sensing by family C G-protein-coupled receptors.

Authors:  P Wellendorph; H Bräuner-Osborne
Journal:  Br J Pharmacol       Date:  2009-03       Impact factor: 8.739

  1 in total

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