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Demonstration of mammalian protein O-mannosyltransferase activity: Coexpression of POMT1 and POMT2 required for enzymatic activity

Defects in O-mannosylation of α-dystroglycan are thought to cause certain types of congenital muscular dystrophies with neuronal migration disorders. Among these muscular dystrophies, Walker–Warburg syndrome is caused by mutations in the gene encoding putative protein O-mannosyltransferase 1 (POMT1)...

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Published in:Proc Natl Acad Sci U S A
Main Authors: Manya, Hiroshi, Chiba, Atsuro, Yoshida, Aruto, Wang, Xiaohui, Chiba, Yasunori, Jigami, Yoshifumi, Margolis, Richard U., Endo, Tamao
Format: Artigo
Language:Inglês
Published: National Academy of Sciences 2003
Subjects:
Biological Sciences
Online Access:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC327176/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14699049/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.0307228101
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