Defective mucin-type glycosylation on α-dystroglycan in COG-deficient cells increases its susceptibility to bacterial proteases

Deficiency in subunits of the conserved oligomeric Golgi (COG) complex results in pleiotropic defects in glycosylation and causes congenital disorders in humans. Insight regarding the functional consequences of this defective glycosylation and the identity of specific glycoproteins affected is lacki...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Biol Chem
Prif Awduron: Yu, Seok-Ho, Zhao, Peng, Prabhakar, Pradeep K., Sun, Tiantian, Beedle, Aaron, Boons, Geert-Jan, Moremen, Kelley W., Wells, Lance, Steet, Richard
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Biochemistry and Molecular Biology 2018
Pynciau:
Glycobiology and Extracellular Matrices
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6139567/
https://ncbi.nlm.nih.gov/pubmed/30049793
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA118.003014
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