MAPKAP1 – Wikipedia
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From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Target of rapamycin complex 2 subunit MAPKAP1 is a protein that in humans is encoded by the MAPKAP1 gene.[5][6] As the name indicates, it is a subunit of mTOR complex 2.
This gene encodes a protein that is highly similar to the yeast SIN1 protein, a stress-activated protein kinase. Alternatively spliced transcript variants encoding distinct isoforms have been described. Alternate polyadenylation sites as well as alternate 3′ UTRs have been identified for transcripts of this gene.[6]
References[edit]
Further reading[edit]
- Colicelli J, Nicolette C, Birchmeier C, et al. (1991). “Expression of three mammalian cDNAs that interfere with RAS function in Saccharomyces cerevisiae”. Proc. Natl. Acad. Sci. U.S.A. 88 (7): 2913–7. Bibcode:1991PNAS…88.2913C. doi:10.1073/pnas.88.7.2913. PMC 51350. PMID 1849280.
- 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): 16899–903. Bibcode:2002PNAS…9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- 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): 1436–50. doi:10.1016/j.cub.2004.07.051. PMID 15324660. S2CID 2371325.
- 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): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Schroder W, Bushell G, Sculley T (2005). “The human stress-activated protein kinase-interacting 1 gene encodes JNK-binding proteins”. Cell. Signal. 17 (6): 761–7. doi:10.1016/j.cellsig.2004.10.015. PMID 15722200.
- Benzinger A, Muster N, Koch HB, et al. (2005). “Targeted proteomic analysis of 14-3-3 sigma, a p53 effector commonly silenced in cancer”. Mol. Cell. Proteomics. 4 (6): 785–95. doi:10.1074/mcp.M500021-MCP200. PMID 15778465.
- Cheng J, Zhang D, Kim K, et al. (2005). “Mip1, an MEKK2-Interacting Protein, Controls MEKK2 Dimerization and Activation”. Mol. Cell. Biol. 25 (14): 5955–64. doi:10.1128/MCB.25.14.5955-5964.2005. PMC 1168836. PMID 15988011.
- Venables JP, Bourgeois CF, Dalgliesh C, et al. (2005). “Up-regulation of the ubiquitous alternative splicing factor Tra2beta causes inclusion of a germ cell-specific exon”. Hum. Mol. Genet. 14 (16): 2289–303. doi:10.1093/hmg/ddi233. PMID 16000324.
- Rual JF, Venkatesan K, Hao T, et al. (2005). “Towards a proteome-scale map of the human protein-protein interaction network”. Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.
- Frias MA, Thoreen CC, Jaffe JD, et al. (2006). “mSin1 is necessary for Akt/PKB phosphorylation, and its isoforms define three distinct mTORC2s”. Curr. Biol. 16 (18): 1865–70. doi:10.1016/j.cub.2006.08.001. PMID 16919458. S2CID 8239162.
- Jacinto E, Facchinetti V, Liu D, et al. (2006). “SIN1/MIP1 maintains rictor-mTOR complex integrity and regulates Akt phosphorylation and substrate specificity”. Cell. 127 (1): 125–37. doi:10.1016/j.cell.2006.08.033. PMID 16962653. S2CID 230319.
- Yang Q, Inoki K, Ikenoue T, Guan KL (2006). “Identification of Sin1 as an essential TORC2 component required for complex formation and kinase activity”. Genes Dev. 20 (20): 2820–32. doi:10.1101/gad.1461206. PMC 1619946. PMID 17043309.
- Makino C, Sano Y, Shinagawa T, et al. (2007). “Sin1 binds to both ATF-2 and p38 and enhances ATF-2-dependent transcription in an SAPK signaling pathway”. Genes Cells. 11 (11): 1239–51. doi:10.1111/j.1365-2443.2006.01016.x. PMID 17054722. S2CID 10605647.
- Olsen JV, Blagoev B, Gnad F, et al. (2006). “Global, in vivo, and site-specific phosphorylation dynamics in signaling networks”. Cell. 127 (3): 635–48. doi:10.1016/j.cell.2006.09.026. PMID 17081983. S2CID 7827573.
- Schroder WA, Buck M, Cloonan N, et al. (2007). “Human Sin1 contains Ras-binding and pleckstrin homology domains and suppresses Ras signalling”. Cell. Signal. 19 (6): 1279–89. doi:10.1016/j.cellsig.2007.01.013. PMID 17303383.
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