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Structural insights into Parkin substrate lysine targeting from minimal Miro substrates
Hereditary Parkinson’s disease is commonly caused by mutations in the protein kinase PINK1 or the E3 ubiquitin ligase Parkin, which function together to eliminate damaged mitochondria. PINK1 phosphorylates both Parkin and ubiquitin to stimulate ubiquitination of dozens of proteins on the surface of...
Autores principales: | Klosowiak, Julian L., Park, Sungjin, Smith, Kyle P., French, Michael E., Focia, Pamela J., Freymann, Douglas M., Rice, Sarah E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015425/ https://www.ncbi.nlm.nih.gov/pubmed/27605430 http://dx.doi.org/10.1038/srep33019 |
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