Derepression of pathological cardiac genes by members of the CaM kinase superfamily (Q36705529)

15 August 2017

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title

Derepression of pathological cardiac genes by members of the CaM kinase superfamily (English)

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15 August 2017

Timothy A McKinsey

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15 August 2017

publication date

5 December 2006

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15 August 2017

published in

Cardiovascular Research

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15 August 2017

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15 August 2017

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15 August 2017

page(s)

667-677

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Mechanisms and models in heart failure: the biomechanical model and beyond

15 August 2017

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CaM kinase II selectively signals to histone deacetylase 4 during cardiomyocyte hypertrophy

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A small molecular activator of cardiac hypertrophy uncovered in a chemical screen for modifiers of the calcineurin signaling pathway

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Roles of cardiac transcription factors in cardiac hypertrophy

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The transcriptional corepressor MITR is a signal-responsive inhibitor of myogenesis

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Identification of a transcriptional repressor related to the noncatalytic domain of histone deacetylases 4 and 5

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Association of COOH-terminal-binding protein (CtBP) and MEF2-interacting transcription repressor (MITR) contributes to transcriptional repression of the MEF2 transcription factor

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Signal-dependent nuclear export of a histone deacetylase regulates muscle differentiation

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Regulation of cardiac stress signaling by protein kinase d1.

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Essential role for protein kinase D family kinases in the regulation of class II histone deacetylases in B lymphocytes

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21 January 2018

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Activation of protein kinase D by signaling through Rho and the alpha subunit of the heterotrimeric G protein G13.

21 January 2018

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Cooperation of Gq, Gi, and G12/13 in protein kinase D activation and phosphorylation induced by lysophosphatidic acid

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Statin therapy for cardiac hypertrophy and heart failure

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Role of the regulatory domain of protein kinase D2 in phorbol ester binding, catalytic activity, and nucleocytoplasmic shuttling

21 January 2018

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Regulated nucleocytoplasmic transport of protein kinase D in response to G protein-coupled receptor activation

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Protein kinase C nu/protein kinase D3 nuclear localization, catalytic activation, and intracellular redistribution in response to G protein-coupled receptor agonists

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Activation loop Ser744 and Ser748 in protein kinase D are transphosphorylated in vivo.

21 January 2018

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Protein kinase C phosphorylates protein kinase D activation loop Ser744 and Ser748 and releases autoinhibition by the pleckstrin homology domain.

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Protein kinase C-dependent protein kinase D activation modulates ERK signal pathway and endothelial cell proliferation by vascular endothelial growth factor

21 January 2018

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Dual phospholipase C/diacylglycerol requirement for protein kinase D1 activation in lymphocytes.

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Tyrosine phosphorylation of protein kinase D in the pleckstrin homology domain leads to activation

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Protein kinase D mediates a stress-induced NF-kappaB activation and survival pathway

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Gbetagamma-mediated regulation of Golgi organization is through the direct activation of protein kinase D

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AKAP-Lbc nucleates a protein kinase D activation scaffold

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PKCepsilon-PKD1 signaling complex at Z-discs plays a pivotal role in the cardiac hypertrophy induced by G-protein coupling receptor agonists

21 January 2018

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Identification and cloning of Kidins220, a novel neuronal substrate of protein kinase D.

21 January 2018

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Protein kinase D regulates vesicular transport by phosphorylating and activating phosphatidylinositol-4 kinase IIIbeta at the Golgi complex

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Regulation of type II PIP kinase by PKD phosphorylation

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Interaction between protein kinase Cmu and the vanilloid receptor type 1.

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A phosphorylation state-specific antibody recognizes Hsp27, a novel substrate of protein kinase D.

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Protein kinase D is a novel mediator of cardiac troponin I phosphorylation and regulates myofilament function

21 January 2018

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Protein kinase D1 and the beta 1 integrin cytoplasmic domain control beta 1 integrin function via regulation of Rap1 activation.

21 January 2018

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The cardiac fibroblast: therapeutic target in myocardial remodeling and failure

21 January 2018

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Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy

21 January 2018

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Angiotensin II-mediated protein kinase D activation stimulates aldosterone and cortisol secretion in H295R human adrenocortical cells.

21 January 2018

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Protein kinase D regulates the fission of cell surface destined transport carriers from the trans-Golgi network

21 January 2018

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Protein kinase D potentiates DNA synthesis and cell proliferation induced by bombesin, vasopressin, or phorbol esters in Swiss 3T3 cells

21 January 2018

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Protein kinase Cmu downregulation of tumor-necrosis-factor-induced apoptosis correlates with enhanced expression of nuclear-factor-kappaB-dependent protective genes

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Protein kinase D protects against oxidative stress-induced intestinal epithelial cell injury via Rho/ROK/PKC-delta pathway activation

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Protein kinase D specifically mediates apoptosis signal-regulating kinase 1-JNK signaling induced by H2O2 but not tumor necrosis factor

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Protein kinase D: a family affair

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Structure of the autoinhibited kinase domain of CaMKII and SAXS analysis of the holoenzyme

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Structure-function of the multifunctional Ca2+/calmodulin-dependent protein kinase II.

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Cardiomyocyte calcium and calcium/calmodulin-dependent protein kinase II: friends or foes?

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Targeted expression of calmodulin increases ventricular cardiomyocyte proliferation and deoxyribonucleic acid synthesis during mouse development.

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Targeted developmental overexpression of calmodulin induces proliferative and hypertrophic growth of cardiomyocytes in transgenic mice.

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Local InsP3-dependent perinuclear Ca2+ signaling in cardiac myocyte excitation-transcription coupling

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Inactivation of the myocyte enhancer factor-2 repressor histone deacetylase-5 by endogenous Ca(2+) //calmodulin-dependent kinase II promotes depolarization-mediated cerebellar granule neuron survival

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MAPs, MARKs and microtubule dynamics.

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MARKing tau for tangles and toxicity.

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An overview of the KIN1/PAR-1/MARK kinase family

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MARK, a novel family of protein kinases that phosphorylate microtubule-associated proteins and trigger microtubule disruption

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Protein kinase MARK/PAR-1 is required for neurite outgrowth and establishment of neuronal polarity

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Mammalian PAR-1 determines epithelial lumen polarity by organizing the microtubule cytoskeleton

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C-TAK1 regulates Ras signaling by phosphorylating the MAPK scaffold, KSR1

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EMK protein kinase-null mice: dwarfism and hypofertility associated with alterations in the somatotrope and prolactin pathways.

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Immune system dysfunction and autoimmune disease in mice lacking Emk (Par-1) protein kinase.

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Regulation of the polarity kinases PAR-1/MARK by 14-3-3 interaction and phosphorylation

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LKB1 is a master kinase that activates 13 kinases of the AMPK subfamily, including MARK/PAR-1

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Comprehensive proteomic analysis of human Par protein complexes reveals an interconnected protein network

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LKB1 is the upstream kinase in the AMP-activated protein kinase cascade

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MARKK, a Ste20-like kinase, activates the polarity-inducing kinase MARK/PAR-1

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GSK-3beta directly phosphorylates and activates MARK2/PAR-1.

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Atypical PKC phosphorylates PAR-1 kinases to regulate localization and activity

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Microtubule affinity-regulating kinase 2 functions downstream of the PAR-3/PAR-6/atypical PKC complex in regulating hippocampal neuronal polarity

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Activated glycogen synthase-3 beta suppresses cardiac hypertrophy in vivo

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Myocyte Enhancer Factors 2A and 2C Induce Dilated Cardiomyopathy in Transgenic Mice

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Protein kinase D directly phosphorylates histone deacetylase 5 via a random sequential kinetic mechanism

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10.1016/J.CARDIORES.2006.11.036

21 January 2018

Identifiers

DOI

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15 August 2017

1 reference