CGMP-dependent protein kinase

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protein kinase, cGMP-dependent, type I
CGMP-dependent.png
Crystallographic structure of the leucine zipper domain of human cGMP dependent protein kinase I beta. [1]
Identifiers
Symbol PRKG1
Alt. symbolsPRKGR1B, PRKG1B
NCBI gene 5592
HGNC 9414
OMIM 176894
RefSeq NM_006258
UniProt Q13976
Other data
Locus Chr. 10 q11.2
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Structures Swiss-model
Domains InterPro
protein kinase, cGMP-dependent, type II
Identifiers
SymbolPRKG2
NCBI gene 5593
HGNC 9416
OMIM 601591
RefSeq NM_006259
UniProt Q13237
Other data
Locus Chr. 4 q13.1-21.1
Search for
Structures Swiss-model
Domains InterPro

cGMP-dependent protein kinase or protein kinase G (PKG) is a serine/threonine-specific protein kinase that is activated by cGMP. It phosphorylates a number of biologically important targets and is implicated in the regulation of smooth muscle relaxation, platelet function, sperm metabolism, cell division, and nucleic acid synthesis.

Contents

Genes and proteins

PKG are serine/threonine kinases that are present in a variety of eukaryotes ranging from the unicellular organism Paramecium to humans. Two PKG genes, coding for PKG type I (PKG-I) and type II (PKG-II), have been identified in mammals. The N-terminus of PKG-I is encoded by two alternatively spliced exons that specify for the PKG-Iα and PKG-Iβ isoforms. PKG-Iβ is activated at ~10-fold higher cGMP concentrations than PKG-Iα. The PKG-I and PKG-II are homodimers of two identical subunits (~75 kDa and ~85 kDa, respectively) and share common structural features.

Each subunit is composed of three functional domains:

Binding of cGMP to the regulatory domain induces a conformational change which stops the inhibition of the catalytic core by the N-terminus and allows the phosphorylation of substrate proteins. Whereas PKG-I is predominantly localized in the cytoplasm, PKG-II is anchored to the plasma membrane by N-terminal myristoylation.

Tissue distribution

In general, PKG-I and PKG-II are expressed in different cell types.

Specifically, in smooth muscle tissue, PKG promotes the opening of calcium-activated potassium channels, leading to cell hyperpolarization and relaxation, and blocks agonist activity of phospholipase C, reducing liberation of stored calcium ions by inositol triphosphate.

Role in cancer

Cancerous colon cells stop producing PKG, which apparently limits beta-catenin, thus allowing the VEGF enzyme to solicit angiogenesis. [2]

Behavioral genetics in Drosophila melanogaster

In Drosophila melanogaster the foraging (for) gene is a polymorphic trait that underlies differences in food-seeking behaviors. The for locus is made up of Rover (forR) and Sitter (forS) alleles, with the Rover allele being dominant. Rover individuals typically travel greater distances when foraging for food, while Sitter individuals travel less distance to forage for food. Both Rover and Sitter phenotypes are considered wild-type, as fruit fly populations typically exhibit a 70:30 Rover-to-Sitter ratio. [3] The Rover and Sitter alleles are located within the 24A3-5 region of the Drosophila melanogaster polytene chromosome, a region which contains the PKG d2g gene. PKG expression levels account for differences in forR and forS allele frequency and therefore behavior as Rover individuals show higher PKG expression than Sitter individuals, and the Sitter phenotype can be converted to Rover by over-expression of the dg2 gene. [4]

See also

Related Research Articles

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<span class="mw-page-title-main">Protein kinase A</span> Family of enzymes

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<span class="mw-page-title-main">Cyclic guanosine monophosphate</span> Chemical compound

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<span class="mw-page-title-main">Telokin</span> Protein domain

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<span class="mw-page-title-main">Myosin light-chain kinase</span> Class of kinase enzymes

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Phosphodiesterase 1, PDE1, EC 3.1.4.1, systematic name oligonucleotide 5′-nucleotidohydrolase) is a phosphodiesterase enzyme also known as calcium- and calmodulin-dependent phosphodiesterase. It is one of the 11 families of phosphodiesterase (PDE1-PDE11). Phosphodiesterase 1 has three subtypes, PDE1A, PDE1B and PDE1C which divide further into various isoforms. The various isoforms exhibit different affinities for cAMP and cGMP.

<span class="mw-page-title-main">Endothelial NOS</span> Protein and coding gene in humans

Endothelial NOS (eNOS), also known as nitric oxide synthase 3 (NOS3) or constitutive NOS (cNOS), is an enzyme that in humans is encoded by the NOS3 gene located in the 7q35-7q36 region of chromosome 7. This enzyme is one of three isoforms that synthesize nitric oxide (NO), a small gaseous and lipophilic molecule that participates in several biological processes. The other isoforms include neuronal nitric oxide synthase (nNOS), which is constitutively expressed in specific neurons of the brain and inducible nitric oxide synthase (iNOS), whose expression is typically induced in inflammatory diseases. eNOS is primarily responsible for the generation of NO in the vascular endothelium, a monolayer of flat cells lining the interior surface of blood vessels, at the interface between circulating blood in the lumen and the remainder of the vessel wall. NO produced by eNOS in the vascular endothelium plays crucial roles in regulating vascular tone, cellular proliferation, leukocyte adhesion, and platelet aggregation. Therefore, a functional eNOS is essential for a healthy cardiovascular system.

<span class="mw-page-title-main">ROCK1</span> Protein

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<span class="mw-page-title-main">AKT3</span> Protein-coding gene in the species Homo sapiens

RAC-gamma serine/threonine-protein kinase is an enzyme that in humans is encoded by the AKT3 gene.

<span class="mw-page-title-main">Myosin-light-chain phosphatase</span>

Myosin light-chain phosphatase, also called myosin phosphatase (EC 3.1.3.53; systematic name [myosin-light-chain]-phosphate phosphohydrolase), is an enzyme (specifically a serine/threonine-specific protein phosphatase) that dephosphorylates the regulatory light chain of myosin II:

<span class="mw-page-title-main">CAMK2G</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">Protein kinase D1</span> Protein-coding gene in the species Homo sapiens

Serine/threonine-protein kinase D1 is an enzyme that in humans is encoded by the PRKD1 gene.

<span class="mw-page-title-main">PRKG1</span> Protein-coding gene in the species Homo sapiens

cGMP-dependent protein kinase 1, alpha isozyme is an enzyme that in humans is encoded by the PRKG1 gene.

<span class="mw-page-title-main">Rho-associated protein kinase</span>

Rho-associated protein kinase (ROCK) is a kinase belonging to the AGC family of serine-threonine specific protein kinases. It is involved mainly in regulating the shape and movement of cells by acting on the cytoskeleton.

Phosphodiesterases (PDEs) are a superfamily of enzymes. This superfamily is further classified into 11 families, PDE1 - PDE11, on the basis of regulatory properties, amino acid sequences, substrate specificities, pharmacological properties and tissue distribution. Their function is to degrade intracellular second messengers such as cyclic adenine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) which leads to several biological processes like effect on intracellular calcium level by the Ca2+ pathway.

References

  1. PDB: 3NMD ; Casteel DE, Smith-Nguyen EV, Sankaran B, Roh SH, Pilz RB, Kim C (October 2010). "A crystal structure of the cyclic GMP-dependent protein kinase I{beta} dimerization/docking domain reveals molecular details of isoform-specific anchoring". The Journal of Biological Chemistry. 285 (43): 32684–8. doi: 10.1074/jbc.C110.161430 . PMC   2963381 . PMID   20826808.
  2. Kwon IK, Schoenlein PV, Delk J, Liu K, Thangaraju M, Dulin NO, et al. (April 2008). "Expression of cyclic guanosine monophosphate-dependent protein kinase in metastatic colon carcinoma cells blocks tumor angiogenesis". Cancer. 112 (7): 1462–70. doi: 10.1002/cncr.23334 . PMID   18260092. S2CID   4763327.
  3. Sokolowski MB (November 2001). "Drosophila: genetics meets behaviour". Nature Reviews. Genetics. 2 (11): 879–90. doi:10.1038/35098592. PMID   11715043. S2CID   13152094.
  4. Osborne KA, Robichon A, Burgess E, Butland S, Shaw RA, Coulthard A, et al. (August 1997). "Natural behavior polymorphism due to a cGMP-dependent protein kinase of Drosophila". Science. 277 (5327): 834–6. doi:10.1126/science.277.5327.834. PMID   9242616.