6GLC

Structure of phospho-Parkin bound to phospho-ubiquitin

6GLC の概要

• エントリーDOI: 10.2210/pdb6glc/pdb
• 分子名称: E3 ubiquitin-protein ligase parkin, Polyubiquitin-B, ZINC ION, ... (7 entities in total)
• 機能のキーワード: ubiquitin, parkin, phospho-ubiquitin, parkinson's disease, e3 ligase, rbr domain, mitophagy, ligase
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 52532.38

構造登録者

Gladkova, C.,Maslen, S.L.,Skehel, J.M.,Komander, D. (登録日: 2018-05-23, 公開日: 2018-06-13, 最終更新日: 2024-10-16)

主引用文献

Gladkova, C.,Maslen, S.L.,Skehel, J.M.,Komander, D.
Mechanism of parkin activation by PINK1.
Nature, 559:410-414, 2018

PubMed Abstract: Mutations in the E3 ubiquitin ligase parkin (PARK2, also known as PRKN) and the protein kinase PINK1 (also known as PARK6) are linked to autosomal-recessive juvenile parkinsonism (AR-JP); at the cellular level, these mutations cause defects in mitophagy, the process that organizes the destruction of damaged mitochondria. Parkin is autoinhibited, and requires activation by PINK1, which phosphorylates Ser65 in ubiquitin and in the parkin ubiquitin-like (Ubl) domain. Parkin binds phospho-ubiquitin, which enables efficient parkin phosphorylation; however, the enzyme remains autoinhibited with an inaccessible active site. It is unclear how phosphorylation of parkin activates the molecule. Here we follow the activation of full-length human parkin by hydrogen-deuterium exchange mass spectrometry, and reveal large-scale domain rearrangement in the activation process, during which the phospho-Ubl rebinds to the parkin core and releases the catalytic RING2 domain. A 1.8 Å crystal structure of phosphorylated human parkin reveals the binding site of the phospho-Ubl on the unique parkin domain (UPD), involving a phosphate-binding pocket lined by AR-JP mutations. Notably, a conserved linker region between Ubl and the UPD acts as an activating element (ACT) that contributes to RING2 release by mimicking RING2 interactions on the UPD, explaining further AR-JP mutations. Our data show how autoinhibition in parkin is resolved, and suggest a mechanism for how parkin ubiquitinates its substrates via an untethered RING2 domain. These findings open new avenues for the design of parkin activators for clinical use.

PubMed: 29995846
DOI: 10.1038/s41586-018-0224-x

実験手法

X-RAY DIFFRACTION (1.8 Å)