The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan

A defect in O-mannosyl glycan is the cause of α-dystroglycanopathy, a group of congenital muscular dystrophies caused by aberrant α-dystroglycan (α-DG) glycosylation. Recently, the entire structure of O-mannosyl glycan, [3GlcAβ1-3Xylα1](n)-3GlcAβ1-4Xyl-Rbo5P-1Rbo5P-3GalNAcβ1-3GlcNAcβ1-4 (phospho-6)M...

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Detalhes bibliográficos
Publicado no:J Biol Chem
Main Authors: Manya, Hiroshi, Yamaguchi, Yoshiki, Kanagawa, Motoi, Kobayashi, Kazuhiro, Tajiri, Michiko, Akasaka-Manya, Keiko, Kawakami, Hiroko, Mizuno, Mamoru, Wada, Yoshinao, Toda, Tatsushi, Endo, Tamao
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2016
Assuntos:
Glycobiology and Extracellular Matrices
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5114413/
https://ncbi.nlm.nih.gov/pubmed/27733679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M116.751917
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