7BII

Crystal structure of Nematocida HUWE1

7BII の概要

• エントリーDOI: 10.2210/pdb7bii/pdb
• 分子名称: E3 ubiquitin-protein ligase HUWE1 (1 entity in total)
• 機能のキーワード: hect e3 ligase, ubiquitin, protein quality control, ligase
• 由来する生物種: Nematocida sp. ERTm5
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 575746.75

構造登録者

Grabarczyk, D.B.,Petrova, O.A.,Meinhart, A.,Kessler, D.,Clausen, T. (登録日: 2021-01-12, 公開日: 2021-07-28, 最終更新日: 2024-01-31)

主引用文献

Grabarczyk, D.B.,Petrova, O.A.,Deszcz, L.,Kurzbauer, R.,Murphy, P.,Ahel, J.,Vogel, A.,Gogova, R.,Faas, V.,Kordic, D.,Schleiffer, A.,Meinhart, A.,Imre, R.,Lehner, A.,Neuhold, J.,Bader, G.,Stolt-Bergner, P.,Bottcher, J.,Wolkerstorfer, B.,Fischer, G.,Grishkovskaya, I.,Haselbach, D.,Kessler, D.,Clausen, T.
HUWE1 employs a giant substrate-binding ring to feed and regulate its HECT E3 domain.
Nat.Chem.Biol., 17:1084-1092, 2021

PubMed Abstract: HUWE1 is a universal quality-control E3 ligase that marks diverse client proteins for proteasomal degradation. Although the giant HECT enzyme is an essential component of the ubiquitin-proteasome system closely linked with severe human diseases, its molecular mechanism is little understood. Here, we present the crystal structure of Nematocida HUWE1, revealing how a single E3 enzyme has specificity for a multitude of unrelated substrates. The protein adopts a remarkable snake-like structure, where the C-terminal HECT domain heads an extended alpha-solenoid body that coils in on itself and houses various protein-protein interaction modules. Our integrative structural analysis shows that this ring structure is highly dynamic, enabling the flexible HECT domain to reach protein targets presented by the various acceptor sites. Together, our data demonstrate how HUWE1 is regulated by its unique structure, adapting a promiscuous E3 ligase to selectively target unassembled orphan proteins.

PubMed: 34294896
DOI: 10.1038/s41589-021-00831-5

実験手法

X-RAY DIFFRACTION (3.037 Å)