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Publication year
2010Source
Cellular and Molecular Life Sciences, 67, 6, (2010), pp. 875-90ISSN
Annotation
01 maart 2010
Publication type
Article / Letter to editor

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Organization
Laboratory of Genetic, Endocrine and Metabolic Diseases
CMBI
Paediatrics - OUD tm 2017
Journal title
Cellular and Molecular Life Sciences
Volume
vol. 67
Issue
iss. 6
Page start
p. 875
Page end
p. 90
Subject
IGMD 8: Mitochondrial medicine; NCMLS 2: Immune Regulation; NCMLS 4: Energy and redox metabolism; NCMLS 4: Energy and redox metabolism IGMD 8: Mitochondrial medicine; NCMLS 6: Genetics and epigenetic pathways of disease; NCMLS 7: Chemical and physical biology; ONCOL 3: Translational researchAbstract
The alpha-kinase family represents a class of atypical protein kinases that display little sequence similarity to conventional protein kinases. Early studies on myosin heavy chain kinases in Dictyostelium discoideum revealed their unusual propensity to phosphorylate serine and threonine residues in the context of an alpha-helix. Although recent studies show that some members of this family can also phosphorylate residues in non-helical regions, the name alpha-kinase has remained. During evolution, the alpha-kinase domains combined with many different functional subdomains such as von Willebrand factor-like motifs (vWKa) and even cation channels (TRPM6 and TRPM7). As a result, these kinases are implicated in a large variety of cellular processes such as protein translation, Mg(2+) homeostasis, intracellular transport, cell migration, adhesion, and proliferation. Here, we review the current state of knowledge on different members of this kinase family and discuss the potential use of alpha-kinases as drug targets in diseases such as cancer.
This item appears in the following Collection(s)
- Academic publications [234109]
- Electronic publications [116863]
- Faculty of Medical Sciences [89175]
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