Full-length huntingtin is palmitoylated at multiple sites and post-translationally myristoylated following caspase-cleavage
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DOI: 10.3389/fphys.2023.1086112
Abstract: Introduction: Huntington disease is an autosomal dominant neurodegenerative disorder which is caused by a CAG repeat expansion in the HTT gene that codes for an elongated polyglutamine tract in the huntingtin (HTT) protein. Huntingtin is… read more here.
Keywords: full length; huntingtin; caspase cleavage; huntingtin palmitoylated ... See more keywords