7QO6

26S proteasome Rpt1-RK -Ubp6-UbVS complex in the s2 state

これはPDB形式変換不可エントリーです。

7QO6 の概要

• エントリーDOI: 10.2210/pdb7qo6/pdb
• EMDBエントリー: 14085
• 分子名称: BJ4_G0020160.mRNA.1.CDS.1, Proteasome endopeptidase complex, Proteasome subunit beta, ... (38 entities in total)
• 機能のキーワード: proteasome, ubiquitin, ubp6, allostery, deubiquitination, motor protein
• 由来する生物種: Saccharomyces cerevisiae (baker's yeast); 詳細
• タンパク質・核酸の鎖数: 49
• 化学式量合計: 1761616.46

構造登録者

Hung, K.Y.S.,Klumpe, S.,Eisele, M.R.,Elsasser, S.,Geng, T.T.,Cheng, T.C.,Joshi, T.,Rudack, T.,Sakata, E.,Finley, D. (登録日: 2021-12-23, 公開日: 2022-03-16, 最終更新日: 2025-10-01)

主引用文献

Hung, K.Y.S.,Klumpe, S.,Eisele, M.R.,Elsasser, S.,Tian, G.,Sun, S.,Moroco, J.A.,Cheng, T.C.,Joshi, T.,Seibel, T.,Van Dalen, D.,Feng, X.H.,Lu, Y.,Ovaa, H.,Engen, J.R.,Lee, B.H.,Rudack, T.,Sakata, E.,Finley, D.
Allosteric control of Ubp6 and the proteasome via a bidirectional switch.
Nat Commun, 13:838-838, 2022

PubMed Abstract: The proteasome recognizes ubiquitinated proteins and can also edit ubiquitin marks, allowing substrates to be rejected based on ubiquitin chain topology. In yeast, editing is mediated by deubiquitinating enzyme Ubp6. The proteasome activates Ubp6, whereas Ubp6 inhibits the proteasome through deubiquitination and a noncatalytic effect. Here, we report cryo-EM structures of the proteasome bound to Ubp6, based on which we identify mutants in Ubp6 and proteasome subunit Rpt1 that abrogate Ubp6 activation. The Ubp6 mutations define a conserved region that we term the ILR element. The ILR is found within the BL1 loop, which obstructs the catalytic groove in free Ubp6. Rpt1-ILR interaction opens the groove by rearranging not only BL1 but also a previously undescribed network of three interconnected active-site-blocking loops. Ubp6 activation and noncatalytic proteasome inhibition are linked in that they are eliminated by the same mutations. Ubp6 and ubiquitin together drive proteasomes into a unique conformation associated with proteasome inhibition. Thus, a multicomponent allosteric switch exerts simultaneous control over both Ubp6 and the proteasome.

PubMed: 35149681
DOI: 10.1038/s41467-022-28186-y

実験手法

ELECTRON MICROSCOPY (6.3 Å)