6G2Y

Crystal structure of the p97 D2 domain in a helical split-washer conformation

6G2Y の概要

• エントリーDOI: 10.2210/pdb6g2y/pdb
• 分子名称: Transitional endoplasmic reticulum ATPase, (4S)-2-METHYL-2,4-PENTANEDIOL, DIMETHYL SULFOXIDE, ... (7 entities in total)
• 機能のキーワード: atpase, p97, protein degradation, hydrolase
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 35334.20

構造登録者

Stach, L.,Morgan, R.M.L.,Freemont, P.S. (登録日: 2018-03-23, 公開日: 2019-04-10, 最終更新日: 2024-01-17)

主引用文献

Stach, L.,Morgan, R.M.,Makhlouf, L.,Douangamath, A.,von Delft, F.,Zhang, X.,Freemont, P.S.
Crystal structure of the catalytic D2 domain of the AAA+ ATPase p97 reveals a putative helical split-washer-type mechanism for substrate unfolding.
Febs Lett., 594:933-943, 2020

PubMed Abstract: Several pathologies have been associated with the AAA+ ATPase p97, an enzyme essential to protein homeostasis. Heterozygous polymorphisms in p97 have been shown to cause neurological disease, while elevated proteotoxic stress in tumours has made p97 an attractive cancer chemotherapy target. The cellular processes reliant on p97 are well described. High-resolution structural models of its catalytic D2 domain, however, have proved elusive, as has the mechanism by which p97 converts the energy from ATP hydrolysis into mechanical force to unfold protein substrates. Here, we describe the high-resolution structure of the p97 D2 ATPase domain. This crystal system constitutes a valuable tool for p97 inhibitor development and identifies a potentially druggable pocket in the D2 domain. In addition, its P6 symmetry suggests a mechanism for substrate unfolding by p97. DATABASE: The atomic coordinates and structure factors have been deposited in the PDB database under the accession numbers 6G2V, 6G2W, 6G2X, 6G2Y, 6G2Z and 6G30.

PubMed: 31701538
DOI: 10.1002/1873-3468.13667

実験手法

X-RAY DIFFRACTION (2.153 Å)