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10.1111/febs.13249

http://scihub22266oqcxt.onion/10.1111/febs.13249
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C4672691!4672691!25712550
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suck abstract from ncbi

pmid25712550      FEBS+J 2015 ; 282 (11): 2076-88
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  • Parkin structure and function #MMPMID25712550
  • Seirafi M; Kozlov G; Gehring K
  • FEBS J 2015[Jun]; 282 (11): 2076-88 PMID25712550show ga
  • Mutations in the parkin or PINK1 genes are the leading cause of the autosomal recessive form of Parkinson?s disease. The gene products, the E3 ubiquitin ligase parkin and the serine/threonine kinase PINK1, are neuroprotective proteins, which act together in a mitochondrial quality control pathway. Here, we review the structure of parkin and mechanisms of its autoinhibition and function as a ubiquitin ligase. We present a model for the recruitment and activation of parkin as a key regulatory step in the clearance of depolarized or damaged mitochondria by autophagy (mitophagy). We conclude with a brief overview of other functions of parkin and considerations for drug discovery in the mitochondrial quality control pathway.
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