Biology:PEX26
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Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
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
- ↑ 1.0 1.1 1.2 "The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes". Nature Cell Biology 5 (5): 454–60. May 2003. doi:10.1038/ncb982. PMID 12717447.
- ↑ "Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation". American Journal of Human Genetics 73 (2): 233–46. Aug 2003. doi:10.1086/377004. PMID 12851857.
- ↑ "Entrez Gene: PEX26 peroxisome biogenesis factor 26". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55670.
- ↑ "Towards a proteome-scale map of the human protein-protein interaction network". Nature 437 (7062): 1173–8. Oct 2005. doi:10.1038/nature04209. PMID 16189514. Bibcode: 2005Natur.437.1173R.
Further reading
- "The DNA sequence of human chromosome 22". Nature 402 (6761): 489–95. Dec 1999. doi:10.1038/990031. PMID 10591208. Bibcode: 1999Natur.402..489D.
- "A genome annotation-driven approach to cloning the human ORFeome". Genome Biology 5 (10): R84. 2005. doi:10.1186/gb-2004-5-10-r84. PMID 15461802.
- "Analysis of human Pex19p's domain structure by pentapeptide scanning mutagenesis". Journal of Molecular Biology 346 (5): 1275–86. Mar 2005. doi:10.1016/j.jmb.2005.01.013. PMID 15713480.
- "Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis". American Journal of Human Genetics 76 (6): 987–1007. Jun 2005. doi:10.1086/430637. PMID 15858711.
- "Towards a proteome-scale map of the human protein-protein interaction network". Nature 437 (7062): 1173–8. Oct 2005. doi:10.1038/nature04209. PMID 16189514. Bibcode: 2005Natur.437.1173R.
- "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". The Journal of Biological Chemistry 281 (3): 1317–23. Jan 2006. doi:10.1074/jbc.M510044200. PMID 16257970.
- "Targeting of the tail-anchored peroxisomal membrane proteins PEX26 and PEX15 occurs through C-terminal PEX19-binding sites". Journal of Cell Science 119 (Pt 12): 2508–17. Jun 2006. doi:10.1242/jcs.02979. PMID 16763195.
- "Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p". The Journal of Biological Chemistry 281 (38): 27693–704. Sep 2006. doi:10.1074/jbc.M605159200. PMID 16854980.
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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