PEX26
Template:PBB Peroxisome assembly protein 26 is a protein that in humans is encoded by the PEX26 gene.[1][2][3]
Interactions
PEX26 has been shown to interact with PEX1,[1] PEX6[1] and SUFU.[4]
References
- ^ a b c Matsumoto N, Tamura S, Fujiki Y (May 2003). "The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes". Nat Cell Biol. 5 (5): 454–60. doi:10.1038/ncb982. PMID 12717447.
{{cite journal}}: CS1 maint: multiple names: authors list (link) Cite error: The named reference "pmid12717447" was defined multiple times with different content (see the help page). - ^ Matsumoto N, Tamura S, Furuki S, Miyata N, Moser A, Shimozawa N, Moser HW, Suzuki Y, Kondo N, Fujiki Y (Jul 2003). "Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation". Am J Hum Genet. 73 (2): 233–46. doi:10.1086/377004. PMC 1180364. PMID 12851857.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: PEX26 peroxisome biogenesis factor 26".
- ^ Rual, Jean-François (Oct 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062). England: 1173–8. doi:10.1038/nature04209. PMID 16189514.
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Further reading
- Dunham I; Shimizu N; Roe BA; et al. (1999). "The DNA sequence of human chromosome 22". Nature. 402 (6761): 489–95. doi:10.1038/990031. PMID 10591208.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - Ota T; Suzuki Y; Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - Collins JE; Wright CL; Edwards CA; et al. (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. 5 (10): R84. doi:10.1186/gb-2004-5-10-r84. PMC 545604. PMID 15461802.
{{cite journal}}: Unknown parameter|author-separator=ignored (help)CS1 maint: unflagged free DOI (link) - 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.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - Fransen M; Vastiau I; Brees C; et al. (2005). "Analysis of human Pex19p's domain structure by pentapeptide scanning mutagenesis". J. Mol. Biol. 346 (5): 1275–86. doi:10.1016/j.jmb.2005.01.013. PMID 15713480.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - Weller S; Cajigas I; Morrell J; et al. (2005). "Alternative Splicing Suggests Extended Function of PEX26 in Peroxisome Biogenesis". Am. J. Hum. Genet. 76 (6): 987–1007. doi:10.1086/430637. PMC 1196456. PMID 15858711.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - 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. doi:10.1038/nature04209. PMID 16189514.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - Furuki S; Tamura S; Matsumoto N; et al. (2006). "Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex". J. Biol. Chem. 281 (3): 1317–23. doi:10.1074/jbc.M510044200. PMID 16257970.
{{cite journal}}: Unknown parameter|author-separator=ignored (help)CS1 maint: unflagged free DOI (link) - Halbach A; Landgraf C; Lorenzen S; et al. (2006). "Targeting of the tail-anchored peroxisomal membrane proteins PEX26 and PEX15 occurs through C-terminal PEX19-binding sites". J. Cell. Sci. 119 (Pt 12): 2508–17. doi:10.1242/jcs.02979. PMID 16763195.
{{cite journal}}: Unknown parameter|author-separator=ignored (help) - Tamura S, Yasutake S, Matsumoto N, Fujiki Y (2006). "Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p". J. Biol. Chem. 281 (38): 27693–704. doi:10.1074/jbc.M605159200. PMID 16854980.
{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
External links
- GeneReviews/NCBI/NIH/UW entry on Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum
- OMIM entries on Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum
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