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Casein kinase 1, delta

Protein Kinase
Top mentioned proteins: CAN, V1a, MAPK, Akt, ACID
Papers on Protein Kinase
An Analog-Sensitive Version of the Protein Kinase Slt2 Allows Identification of Novel Targets of the Yeast Cell Wall Integrity Pathway.
Martín et al., Madrid, Spain. In J Biol Chem, Feb 2016
UNASSIGNED: The yeast cell wall integrity (CWI) MAPK Slt2 mediates the transcriptional response to cell wall alterations through phosphorylation of transcription factors Rlm1 and SBF.
Persistent Activation of cGMP-dependent Protein Kinase by a Nitrated Cyclic Nucleotide Via Site-specific Protein S-Guanylation.
Akaike et al., In Biochemistry, Feb 2016
Here, we demonstrate that 8-nitro-cGMP potentially S-guanylates thiol groups of cGMP-dependent protein kinase (PKG), the enzyme that serves as one of the major receptor proteins for intracellular cGMP and controls a variety of cellular responses.
Antiaging Gene Klotho Deficiency Promoted High-Fat Diet-Induced Arterial Stiffening via Inactivation of AMP-Activated Protein Kinase.
Sun et al., United States. In Hypertension, Feb 2016
Protein expressions of phosphorylated AMP-activated protein kinase-α (AMPKα), phosphorylated endothelial nitric oxide synthase (eNOS), and manganese-dependent superoxide dismutase (Mn-SOD) were decreased, whereas protein expressions of collagen I, transforming growth factor-β1, and Runx2 were increased in aortas of KL(+/-) mice fed on HFD.
Protocatechualdehyde Protects Against Cerebral Ischemia-Reperfusion-Induced Oxidative Injury Via Protein Kinase Cε/Nrf2/HO-1 Pathway.
Wen et al., Xi'an, China. In Mol Neurobiol, Feb 2016
Moreover, knockdown of protein kinase Cε (PKCε) also blocked PCA-induced Nfr2 nuclear translocation, HO-1 expression, and neuroprotection.
Regulator of G-Protein Signaling 10 Negatively Regulates Cardiac Remodeling by Blocking Mitogen-Activated Protein Kinase-Extracellular Signal-Regulated Protein Kinase 1/2 Signaling.
Yuan et al., Changsha, China. In Hypertension, Jan 2016
Mechanistically, cardiac remodeling improvement elicited by RGS10 was associated with the abrogation of mitogen-activated protein kinase kinase 1/2-extracellular signal-regulated protein kinase 1/2 signaling.
Extreme Outlier Analysis Identifies Occult Mitogen-Activated Protein Kinase Pathway Mutations in Patients With Low-Grade Serous Ovarian Cancer.
Iyer et al., Houston, United States. In J Clin Oncol, Jan 2016
CONCLUSION: Alterations affecting the mitogen-activated protein kinase pathway are present in the majority of patients with LGS ovarian cancer.
Analysis of Phosphorylation of the Receptor-Like Protein Kinase HAESA during Arabidopsis Floral Abscission.
Walker et al., Columbia, United States. In Plos One, Dec 2015
Through in vitro and in vivo analysis of HAE phosphorylation, we provide evidence that a conserved phosphorylation site on a region of the HAE protein kinase domain known as the activation segment positively regulates HAE activity.
Mitogen-Activated Protein Kinase Kinase 4 Gene Polymorphism and Cancer Risk.
Liang et al., Chongqing, China. In Medicine (baltimore), Nov 2015
A number of epidemiological studies have assessed the association of -1304T > G polymorphism in the MKK4 gene and risk of cancer, but the results lack of statistical power due to the limited subjects used in these studies.
Counteracting Protein Kinase Activity in the Heart: The Multiple Roles of Protein Phosphatases.
El-Armouche et al., Dresden, Germany. In Front Pharmacol, 2014
Decades of cardiovascular research have shown that variable and flexible levels of protein phosphorylation are necessary to maintain cardiac function.
Post-translational modifications of voltage-gated sodium channels in chronic pain syndromes.
Decosterd et al., Boston, United States. In Front Pharmacol, 2014
In this review we will discuss the role of Protein Kinase A, B, and C, Mitogen Activated Protein Kinases and Ca++/Calmodulin-dependent Kinase II in peripheral chronic pain syndromes.
The Receptor for Activated C Kinase in Plant Signaling: Tale of a Promiscuous Little Molecule.
Villanueva et al., Ecatepec, Mexico. In Front Plant Sci, 2014
Although RACK1 proteins maintain conserved Protein Kinase C binding sites, the lack of a bona fide PKC adds complexity and enigma to the nature of the ligand partners with which RACK1 interacts in plants.
Drosophila and vertebrate casein kinase Idelta exhibits evolutionary conservation of circadian function.
Price et al., Kansas City, United States. In Genetics, 2009
The results demonstrate a high degree of evolutionary conservation of fly and vertebrate CKIdelta and of the functions affected by their period-shortening mutations.
Drosophila Smoothened phosphorylation sites essential for Hedgehog signal transduction.
Tomlinson et al., New York City, United States. In Nat Cell Biol, 2005
Together, Protein Kinase A, Casein Kinase 1 and Glycogen Synthase Kinase 3 silence the pathway in the absence of ligand by phosphorylating Ci at a defined cluster of sites, thereby promoting its proteolytic conversion to a transcriptional repressor (Ci-75).
Proteolysis of the Hedgehog signaling effector Cubitus interruptus requires phosphorylation by Glycogen Synthase Kinase 3 and Casein Kinase 1.
Kalderon et al., New York City, United States. In Cell, 2002
Ci-155 proteolysis depends on phosphorylation at three sites by Protein Kinase A (PKA).
Protein kinase D regulates the fission of cell surface destined transport carriers from the trans-Golgi network.
Malhotra et al., San Diego, United States. In Cell, 2001
When a kinase inactive form of Protein Kinase D (PKD-K618N) was expressed in HeLa cells, it localized to the trans-Golgi network (TGN) and caused extensive tubulation.
Analogs of cyclic adenosine monophosphate: correlation of inhibition of Purkinje Neurons with Protein Kinase Activation.
Henriksen et al., In Science, 1975
with their reported potency in activating cyclic AMP-dependent protein kinase.
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