Literature DB >> 15970481

Molecular properties of mammalian proteins that interact with cGMP: protein kinases, cation channels, phosphodiesterases, and multi-drug anion transporters.

Sharron H Francis1, Mitsi A Blount, Roya Zoraghi, Jackie D Corbin.   

Abstract

Cyclic GMP is a critical second messenger signaling molecule in many mammalian cell types. It is synthesized by a family of guanylyl cyclases that is activated in response to stimuli from hormones such as natriuretic peptides, members of the guanylin family, and chemical stimuli including nitric oxide and carbon monoxide. The resulting elevation of cGMP modulates myriad physiological processes. Three major groups of cellular proteins bind cGMP specifically at allosteric sites; interaction of cGMP with these sites modulates the activities and functions of other domains within these protein groups to bring about physiological effects. These proteins include the cyclic nucleotide (cN)-dependent protein kinases, cN-gated cation channels, and cGMP-binding phosphodiesterases (PDE). Cyclic GMP also interacts with the catalytic sites of many cN PDEs and with some members of the multi-drug anion transporter family (MRPs) which can extrude nucleotides from cells. The allosteric cN-binding sites in the kinases and the cN-gated channels are evolutionarily and biochemically related, whereas the allosteric cGMP-binding sites in PDEs (also known as GAF domains), the catalytic sites of PDEs , and the ligand-binding sites in the MRPs are evolutionarily and biochemically distinct from each other and from those in the kinase and channel families. The sites that interact with cGMP within each of these groups of proteins have unique properties that provide for cGMP binding. Within a given cell, cGMP can potentially interact with members of all these groups of proteins if they are present. The relative abundance and affinities of these various cGMP-binding sites in conjunction with their subcellular compartmentation, proximity to cyclases and PDEs, and post-translational modification contribute importantly in determining the impact of these respective proteins to cGMP signaling within a particular cell.

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Year:  2005        PMID: 15970481     DOI: 10.2741/1684

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  17 in total

Review 1.  cGMP-dependent protein kinases and cGMP phosphodiesterases in nitric oxide and cGMP action.

Authors:  Sharron H Francis; Jennifer L Busch; Jackie D Corbin; David Sibley
Journal:  Pharmacol Rev       Date:  2010-09       Impact factor: 25.468

2.  Inactivation of nitric oxide by rat cerebellar slices.

Authors:  C N Hall; J Garthwaite
Journal:  J Physiol       Date:  2006-09-14       Impact factor: 5.182

Review 3.  Genetically encodable fluorescent biosensors for tracking signaling dynamics in living cells.

Authors:  Robert H Newman; Matthew D Fosbrink; Jin Zhang
Journal:  Chem Rev       Date:  2011-04-01       Impact factor: 60.622

Review 4.  The multiple actions of NO.

Authors:  Yuansheng Gao
Journal:  Pflugers Arch       Date:  2009-12-19       Impact factor: 3.657

5.  Inhibition of dopamine signaling suppresses cGMP accumulation in rd1 retinal organ cultures.

Authors:  Ju Zhang; Angela M Richmond; Judith M Ogilvie
Journal:  Neuroreport       Date:  2014-05-28       Impact factor: 1.837

6.  An N-terminally truncated form of cyclic GMP-dependent protein kinase Iα (PKG Iα) is monomeric and autoinhibited and provides a model for activation.

Authors:  Thomas M Moon; Jessica L Sheehe; Praveena Nukareddy; Lydia W Nausch; Jessica Wohlfahrt; Dwight E Matthews; Donald K Blumenthal; Wolfgang R Dostmann
Journal:  J Biol Chem       Date:  2018-03-30       Impact factor: 5.157

7.  Differential patterning of cGMP in vascular smooth muscle cells revealed by single GFP-linked biosensors.

Authors:  Lydia W M Nausch; Jonathan Ledoux; Adrian D Bonev; Mark T Nelson; Wolfgang R Dostmann
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-28       Impact factor: 11.205

8.  Real-time monitoring the spatiotemporal dynamics of intracellular cGMP in vascular smooth muscle cells.

Authors:  Kara F Held; Wolfgang R Dostmann
Journal:  Methods Mol Biol       Date:  2013

9.  Protein kinase G regulates the basal tension and plays a major role in nitrovasodilator-induced relaxation of porcine coronary veins.

Authors:  H Qi; X Zheng; X Qin; D Dou; H Xu; J U Raj; Y Gao
Journal:  Br J Pharmacol       Date:  2007-09-24       Impact factor: 8.739

10.  Sildenafil citrate and tamsulosin combination is not superior to monotherapy in treating lower urinary tract symptoms and erectile dysfunction.

Authors:  Altug Tuncel; Varol Nalcacioglu; Kemal Ener; Yilmaz Aslan; Omur Aydin; Ali Atan
Journal:  World J Urol       Date:  2009-10-24       Impact factor: 4.226

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