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Most mutations that cause spinocerebellar ataxia autosomal recessive type 16 (SCAR16) destabilize the protein quality-control E3 ligase CHIP

The accumulation of misfolded proteins promotes protein aggregation and neuronal death in many neurodegenerative diseases. To counteract misfolded protein accumulation, neurons have pathways that recognize and refold or degrade aggregation-prone proteins. One U-box–containing E3 ligase, C terminus o...

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Vydáno v:J Biol Chem
Hlavní autoři: Kanack, Adam J., Newsom, Oliver J., Scaglione, Kenneth Matthew
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Biochemistry and Molecular Biology 2018
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5827432/
https://ncbi.nlm.nih.gov/pubmed/29317501
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA117.000477
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