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Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments.
Honsho M, Yagita Y, Kinoshita N, Fujiki Y. Honsho M, et al. Biochim Biophys Acta. 2008 Oct;1783(10):1857-65. doi: 10.1016/j.bbamcr.2008.05.018. Epub 2008 Jun 3. Biochim Biophys Acta. 2008. PMID: 18571506
The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14p.
Otera H, Harano T, Honsho M, Ghaedi K, Mukai S, Tanaka A, Kawai A, Shimizu N, Fujiki Y. Otera H, et al. J Biol Chem. 2000 Jul 14;275(28):21703-14. doi: 10.1074/jbc.M000720200. J Biol Chem. 2000. PMID: 10767286
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
Ghaedi K, Honsho M, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y. Ghaedi K, et al. Am J Hum Genet. 2000 Oct;67(4):976-81. doi: 10.1086/303086. Epub 2000 Aug 31. Am J Hum Genet. 2000. PMID: 10968777 Free PMC article.
Topogenesis of peroxisomal membrane protein requires a short, positively charged intervening-loop sequence and flanking hydrophobic segments. study using human membrane protein PMP34.
Honsho M, Fujiki Y. Honsho M, et al. J Biol Chem. 2001 Mar 23;276(12):9375-82. doi: 10.1074/jbc.M003304200. Epub 2000 Dec 19. J Biol Chem. 2001. PMID: 11121399
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