The mitochondrial protein BNIP3L is the substrate of PARK2 and mediates mitophagy in PINK1/PARK2 pathway (Q38917518)

7 September 2017

title

The mitochondrial protein BNIP3L is the substrate of PARK2 and mediates mitophagy in PINK1/PARK2 pathway (English)

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7 September 2017

Feng Gao

1

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7 September 2017

Dong Chen

2

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7 September 2017

Jianmin Si

3

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7 September 2017

Qingsong Hu

4

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7 September 2017

Zhenghong Qin

5

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7 September 2017

Ming Fang

6

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7 September 2017

Guanghui Wang

7

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7 September 2017

publication date

22 January 2015

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7 September 2017

published in

Human Molecular Genetics

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7 September 2017

volume

24

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7 September 2017

issue

9

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7 September 2017

page(s)

2528-2538

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Expanding insights of mitochondrial dysfunction in Parkinson's disease.

7 September 2017

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Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin

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PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

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PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria

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Drosophila parkin requires PINK1 for mitochondrial translocation and ubiquitinates mitofusin

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Landscape of the PARKIN-dependent ubiquitylome in response to mitochondrial depolarization

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Broad activation of the ubiquitin-proteasome system by Parkin is critical for mitophagy

21 January 2018

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PINK1 and Parkin target Miro for phosphorylation and degradation to arrest mitochondrial motility

21 January 2018

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Parkin ubiquitinates Drp1 for proteasome-dependent degradation: implication of dysregulated mitochondrial dynamics in Parkinson disease

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21 January 2018

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Parkin Mono-ubiquitinates Bcl-2 and Regulates Autophagy

21 January 2018

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Gp78, an ER associated E3, promotes SOD1 and ataxin-3 degradation.

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDV017

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7 September 2017

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