Solution structure of ubiquitin-like domain of human parkin

Autogenerated by for
Created on Sat, 2016-11-19 12:11, last updated on Sat, 2016-11-19 12:11

Vertical Tabs

QR Code for https://3dprint.nih.gov/discover/3dpx-004179

Rating

No votes yet

Licensing

Comments

Comments

Mutations in this gene are known to cause a familial form of Parkinson's disease known as autosomal recessive juvenile Parkinson's disease (AR-JP). Moreover, Parkin is described to be necessary for mitophagy (autophagy of mitochondria). more