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New insights into the structure of PINK1 and the mechanism of ubiquitin phosphorylation.
Rasool S, Trempe JF. Rasool S, et al. Crit Rev Biochem Mol Biol. 2018 Oct;53(5):515-534. doi: 10.1080/10409238.2018.1491525. Epub 2018 Sep 21. Crit Rev Biochem Mol Biol. 2018. PMID: 30238821 Review.
Mutations in PINK1 cause early-onset recessive Parkinson's disease. This gene encodes a protein kinase implicated in mitochondrial quality control via ubiquitin phosphorylation and activation of the E3 ubiquitin ligase Parkin. ...
Mutations in PINK1 cause early-onset recessive Parkinson's disease. This gene encodes a protein kinase implicated in mitochondrial qu …
PINK1 autophosphorylation is required for ubiquitin recognition.
Rasool S, Soya N, Truong L, Croteau N, Lukacs GL, Trempe JF. Rasool S, et al. EMBO Rep. 2018 Apr;19(4):e44981. doi: 10.15252/embr.201744981. Epub 2018 Feb 23. EMBO Rep. 2018. PMID: 29475881 Free PMC article.
Mutations in PINK1 cause autosomal recessive Parkinson's disease (PD), a neurodegenerative movement disorder. PINK1 is a kinase that acts as a sensor of mitochondrial damage and initiates Parkin-mediated clearance of the damaged organelle. ...
Mutations in PINK1 cause autosomal recessive Parkinson's disease (PD), a neurodegenerative movement disorder. PINK1 is a kinase that …
A Ubl/ubiquitin switch in the activation of Parkin.
Sauvé V, Lilov A, Seirafi M, Vranas M, Rasool S, Kozlov G, Sprules T, Wang J, Trempe JF, Gehring K. Sauvé V, et al. Among authors: rasool s. EMBO J. 2015 Oct 14;34(20):2492-505. doi: 10.15252/embj.201592237. Epub 2015 Aug 7. EMBO J. 2015. PMID: 26254305 Free PMC article.
Mutations in Parkin and PINK1 cause an inherited early-onset form of Parkinson's disease. The two proteins function together in a mitochondrial quality control pathway whereby PINK1 accumulates on damaged mitochondria and activates Parkin to induce mitophagy. ...
Mutations in Parkin and PINK1 cause an inherited early-onset form of Parkinson's disease. The two proteins function together in a mit …