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CLK3 (gene)
Introduction
Dual specificity protein kinase CLK3 is an enzyme that in humans is encoded by the CLK3 gene.[1][2] The CLK3 gene encodes a serine/threonine type protein kinase with a non-conserved N-terminal domain. A long and short isoform (phclk3 and pclk3/152) result from alternative splicing and coexist in different tissues. Isoform phclk3/152 lacks the kinase domain.[3]
References
References
- β Hanes J, von der Kammer H, Klaudiny J, Scheit KH (Jan 1995). “Characterization by cDNA cloning of two new human protein kinases. Evidence by sequence comparison of a new family of mammalian protein kinases”. J Mol Biol. 244 (5): 665β72. doi:10.1006/jmbi.1994.1763. PMIDΒ 7990150.
- β Talmadge CB, Finkernagel S, Sumegi J, Sciorra L, Rabinow L (Dec 1998). “Chromosomal mapping of three human LAMMER protein-kinase-encoding genes”. Hum Genet. 103 (4): 523β4. doi:10.1007/s004390050861. PMIDΒ 9856501.
- β “Entrez Gene: CLK3 CDC-like kinase 3”.
Further reading
Further reading
- Maruyama K, Sugano S (1994). “Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides”. Gene. 138 (1β2): 171β4. doi:10.1016/0378-1119(94)90802-8. PMIDΒ 8125298.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). “Construction and characterization of a full length-enriched and a 5′-end-enriched cDNA library”. Gene. 200 (1β2): 149β56. doi:10.1016/S0378-1119(97)00411-3. PMIDΒ 9373149.
- Duncan PI, Stojdl DF, Marius RM, et al. (1998). “The Clk2 and Clk3 dual-specificity protein kinases regulate the intranuclear distribution of SR proteins and influence pre-mRNA splicing”. Exp. Cell Res. 241 (2): 300β8. doi:10.1006/excr.1998.4083. PMIDΒ 9637771.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899β903. doi:10.1073/pnas.242603899. PMCΒ 139241. PMIDΒ 12477932.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). “Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet. 36 (1): 40β5. doi:10.1038/ng1285. PMIDΒ 14702039.
- Hillman RT, Green RE, Brenner SE (2005). “An unappreciated role for RNA surveillance”. Genome Biol. 5 (2): R8. doi:10.1186/gb-2004-5-2-r8. PMCΒ 395752. PMIDΒ 14759258.
- Jin J, Smith FD, Stark C, et al. (2004). “Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization”. Curr. Biol. 14 (16): 1436β50. doi:10.1016/j.cub.2004.07.051. PMIDΒ 15324660.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121β7. doi:10.1101/gr.2596504. PMCΒ 528928. PMIDΒ 15489334.
- Rual JF, Venkatesan K, Hao T, et al. (2005). “Towards a proteome-scale map of the human protein-protein interaction network”. Nature. 437 (7062): 1173β8. doi:10.1038/nature04209. PMIDΒ 16189514.
- Olsen JV, Blagoev B, Gnad F, et al. (2006). “Global, in vivo, and site-specific phosphorylation dynamics in signaling networks”. Cell. 127 (3): 635β48. doi:10.1016/j.cell.2006.09.026. PMIDΒ 17081983.
- Wissing J, JΓ€nsch L, Nimtz M, et al. (2007). “Proteomics analysis of protein kinases by target class-selective prefractionation and tandem mass spectrometry”. Mol. Cell. Proteomics. 6 (3): 537β47. doi:10.1074/mcp.T600062-MCP200. PMIDΒ 17192257.
External links
External links
- Clk dual-specificity kinases at the US National Library of Medicine Medical Subject Headings (MeSH)
- Human CLK3 genome location and CLK3 gene details page in the UCSC Genome Browser.
