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| Title: | The alpha-kinase family: an exceptional branch on the protein kinase tree. |
| Author(s): | Middelbeek, J.A.J. (314439188) Clark, K. Venselaar, H. (321457250) Huynen, M.A. (298200597) Leeuwen, F.N. van (314437290) |
| Publication year: | 2010 |
| Document type: | Article / Letter to editor |
| Journal: | Cellular Molecular Life Science |
| ISSN: | 1420-682X |
| Volume: | vol. 67 |
| Issue: | iss. 6 |
| Start page: | p. 875 |
| End page: | p. 890 |
| Abstract: | 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. |
| Subject: | IGMD 8: Mitochondrial medicine NCMLS 1B: Immune Regulation NCMLS 2A: Energy and redox metabolism NCMLS 2A: Energy and redox metabolism
IGMD 8: Mitochondrial medicine NCMLS 3A: Genetics and epigenetic pathways of disease NCMLS 3B: Chemical and physical biology ONCOL 3: Translational research |
| Organization: | Laboratory of Genetic, Endocrine and Metabolic Diseases UMCN Extern CMBI Paediatrics |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/88992
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