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The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids

Several orphan G protein-coupled receptors are structurally close to the family of P2Y nucleotide receptors: GPR80/99 and GPR91 are close to P2Y(1/2/4/6/11) receptors, whereas GPR87, H963 and GPR34 are close to P2Y(12/13/14). Over the years, several laboratories have attempted without success to ide...

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Autores principales: Gonzalez, Nathalie Suarez, Communi, Didier, Hannedouche, Sébastien, Boeynaems, Jean-Marie
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096567/
https://www.ncbi.nlm.nih.gov/pubmed/18404396
http://dx.doi.org/10.1007/s11302-004-5071-6
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author Gonzalez, Nathalie Suarez
Communi, Didier
Hannedouche, Sébastien
Boeynaems, Jean-Marie
author_facet Gonzalez, Nathalie Suarez
Communi, Didier
Hannedouche, Sébastien
Boeynaems, Jean-Marie
author_sort Gonzalez, Nathalie Suarez
collection PubMed
description Several orphan G protein-coupled receptors are structurally close to the family of P2Y nucleotide receptors: GPR80/99 and GPR91 are close to P2Y(1/2/4/6/11) receptors, whereas GPR87, H963 and GPR34 are close to P2Y(12/13/14). Over the years, several laboratories have attempted without success to identify the ligands of those receptors. In early 2004, two papers have been published: One claiming that GPR80/99 is an AMP receptor, called P2Y(15), and the other one showing that GPR80/99 is a receptor for α-ketoglutarate, while GPR91 is a succinate receptor. The accompanying paper by Qi et al. entirely supports that GPR80/99 is an α-ketoglutarate receptor and not an AMP receptor. The closeness of dicarboxylic acid and P2Y nucleotide receptors might be linked to the negative charges of both types of ligands and the involvement of conserved Arg residues in their neutralization.
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spelling pubmed-20965672008-02-27 The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids Gonzalez, Nathalie Suarez Communi, Didier Hannedouche, Sébastien Boeynaems, Jean-Marie Purinergic Signal Review Several orphan G protein-coupled receptors are structurally close to the family of P2Y nucleotide receptors: GPR80/99 and GPR91 are close to P2Y(1/2/4/6/11) receptors, whereas GPR87, H963 and GPR34 are close to P2Y(12/13/14). Over the years, several laboratories have attempted without success to identify the ligands of those receptors. In early 2004, two papers have been published: One claiming that GPR80/99 is an AMP receptor, called P2Y(15), and the other one showing that GPR80/99 is a receptor for α-ketoglutarate, while GPR91 is a succinate receptor. The accompanying paper by Qi et al. entirely supports that GPR80/99 is an α-ketoglutarate receptor and not an AMP receptor. The closeness of dicarboxylic acid and P2Y nucleotide receptors might be linked to the negative charges of both types of ligands and the involvement of conserved Arg residues in their neutralization. Springer Netherlands 2004-12 /pmc/articles/PMC2096567/ /pubmed/18404396 http://dx.doi.org/10.1007/s11302-004-5071-6 Text en © Springer 2004
spellingShingle Review
Gonzalez, Nathalie Suarez
Communi, Didier
Hannedouche, Sébastien
Boeynaems, Jean-Marie
The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids
title The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids
title_full The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids
title_fullStr The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids
title_full_unstemmed The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids
title_short The fate of P2Y-related orphan receptors: GPR80/99 and GPR91 are receptors of dicarboxylic acids
title_sort fate of p2y-related orphan receptors: gpr80/99 and gpr91 are receptors of dicarboxylic acids
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2096567/
https://www.ncbi.nlm.nih.gov/pubmed/18404396
http://dx.doi.org/10.1007/s11302-004-5071-6
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