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...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:J Biol Chem
Main Authors: Yu, Seok-Ho, Zhao, Peng, Prabhakar, Pradeep K., Sun, Tiantian, Beedle, Aaron, Boons, Geert-Jan, Moremen, Kelley W., Wells, Lance, Steet, Richard
Format: Artigo
Jezik:Inglês
Izdano: American Society for Biochemistry and Molecular Biology 2018
Teme:
Glycobiology and Extracellular Matrices
Online dostop: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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