Chemical Diversification of Enzymatically Assembled Polyubiquitin Chains to Decipher the Ubiquitin Codes Programmed on the Branch Structure
Takafumi Furuhata(The University of Tokyo), Akimitsu Okamoto(The University of Tokyo), Yusuke Sato(Japan Science and Technology Agency), Shuya Fukai(Tokyo Institute of Technology), Kei Okatsu(Kyoto University), Bumkyu Choi(The University of Tokyo), Taiki Uno(The University of Tokyo), Ryota Shinohara(The University of Tokyo)
Cited by 2
Related Papers
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy
|The Journal of Cell Biology|2010|1.9k
Ubiquitin is phosphorylated by PINK1 to activate parkin
|Nature|2014|1.5k
PINK1 autophosphorylation upon membrane potential dissipation is essential for Parkin recruitment to damaged mitochondria
|Nature Communications|2012|599
p62/SQSTM1 cooperates with Parkin for perinuclear clustering of depolarized mitochondria
|Genes to Cells|2010|390
Phosphorylated ubiquitin chain is the genuine Parkin receptor
|The Journal of Cell Biology|2015|261