The muscular dystrophy gene TMEM5 encodes a ribitol ô1,4-Xylosyltransferase required for the functional glycosylation of dystroglycan

Journal of Biological Chemistry

Volumn 291, Issue 47, 2016, Pages 24618-24627

  Manya, Hiroshi ^a   Yamaguchi, Yoshiki ^b   Kanagawa, Motoi ^c   Kobayashi, Kazuhiro ^c   Tajiri, Michiko ^d   Akasaka Manya, Keiko ^a   Kawakami, Hiroko ^e   Mizuno, Mamoru ^e   Wada, Yoshinao ^d   Toda, Tatsushi ^c   Endo, Tamao ^a,f  

^a Tokyo Metropolitan Institute of Gerontology   (Japan)

^b RIKEN   (Japan)

^c KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^d RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

^e NOGUCHI INSTITUTE   (Japan)

^f NONE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

GENES; GLYCOSYLATION; XYLOSE;

ANOMERIC CONFIGURATION; BIOSYNTHETIC PATHWAY; D-XYLOSE; EXPERIMENTAL EVIDENCE; EXTRACELLULAR MATRICES; GENE PRODUCTS; MUSCULAR DYSTROPHY; NMR ANALYSIS;

POLYSACCHARIDES;

CASPASE 9; CRISPR ASSOCIATED PROTEIN; DYSTROGLYCAN; RIBITOL BETA 1,4 XYLOSYLTRANSFERASE; TRANSFERASE; UNCLASSIFIED DRUG; MEMBRANE PROTEIN; PHOSPHOTRANSFERASE; TMEM5 PROTEIN, HUMAN;

ALPHA DYSTROGLYCANOPATHY; ARTICLE; CONTROLLED STUDY; EMBRYO; ENZYME ACTIVITY; GENE; GENE FUNCTION; GENE IDENTIFICATION; GLYCOSYLATION; HUMAN; HUMAN CELL; IMAGE ANALYSIS; MISSENSE MUTATION; MOLECULAR IMAGING; MUSCULAR DYSTROPHY; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; TMEM5 GENE; CELL LINE; CHEMISTRY; GENETICS; METABOLISM;

CELL LINE; DYSTROGLYCANS; GLYCOSYLATION; HUMANS; MEMBRANE PROTEINS; MUSCULAR DYSTROPHIES; MUTATION, MISSENSE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; TRANSFERASES (OTHER SUBSTITUTED PHOSPHATE GROUPS);

EID: 84995773040     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M116.751917     Document Type: Article

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