Cargando…
The Role of N-Glycosylation in Folding, Trafficking, and Functionality of Lysosomal Protein CLN5
CLN5 is a soluble lysosomal protein with unknown function. Mutations in CLN5 lead to neuronal ceroid lipofuscinosis, a group of inherited neurodegenerative disorders that mainly affect children. CLN5 has eight potential N-glycosylation sites based on the Asn-X-Thr/Ser consensus sequence. Through sit...
Autores principales: | Moharir, Akshay, Peck, Sun H., Budden, Theodore, Lee, Stella Y. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769244/ https://www.ncbi.nlm.nih.gov/pubmed/24058541 http://dx.doi.org/10.1371/journal.pone.0074299 |
Ejemplares similares
-
Autophagy–lysosome pathway alterations and alpha-synuclein up-regulation in the subtype of neuronal ceroid lipofuscinosis, CLN5 disease
por: Adams, Jessie, et al.
Publicado: (2019) -
Deficiency of the Lysosomal Protein CLN5 Alters Lysosomal Function and Movement
por: Basak, Indranil, et al.
Publicado: (2021) -
KCTD7 mutations impair the trafficking of lysosomal enzymes through CLN5 accumulation to cause neuronal ceroid lipofuscinoses
por: Wang, Yalan, et al.
Publicado: (2022) -
Loss of the batten disease protein CLN3 leads to mis-trafficking of M6PR and defective autophagic-lysosomal reformation
por: Calcagni’, Alessia, et al.
Publicado: (2023) -
A lysosomal enigma CLN5 and its significance in understanding neuronal ceroid lipofuscinosis
por: Basak, I., et al.
Publicado: (2021)