3J02

Lidless D386A Mm-cpn in the pre-hydrolysis ATP-bound state

3J02 の概要

• エントリーDOI: 10.2210/pdb3j02/pdb
• 関連するPDBエントリー: 3J03
• EMDBエントリー: 5258
• 分子名称: Lidless D386A Mm-cpn variant (1 entity in total)
• 機能のキーワード: mm-cpn, chaperonin, atp-bound, chaperone
• 由来する生物種: Methanococcus maripaludis
• タンパク質・核酸の鎖数: 16
• 化学式量合計: 841192.43

構造登録者

Zhang, J.,Ma, B.,DiMaio, F.,Douglas, N.R.,Joachimiak, L.,Baker, D.,Frydman, J.,Levitt, M.,Chiu, W. (登録日: 2011-02-10, 公開日: 2011-05-18, 最終更新日: 2024-02-21)

主引用文献

Zhang, J.,Ma, B.,DiMaio, F.,Douglas, N.R.,Joachimiak, L.A.,Baker, D.,Frydman, J.,Levitt, M.,Chiu, W.
Cryo-EM structure of a group II chaperonin in the prehydrolysis ATP-bound state leading to lid closure.
Structure, 19:633-639, 2011

PubMed Abstract: Chaperonins are large ATP-driven molecular machines that mediate cellular protein folding. Group II chaperonins use their "built-in lid" to close their central folding chamber. Here we report the structure of an archaeal group II chaperonin in its prehydrolysis ATP-bound state at subnanometer resolution using single particle cryo-electron microscopy (cryo-EM). Structural comparison of Mm-cpn in ATP-free, ATP-bound, and ATP-hydrolysis states reveals that ATP binding alone causes the chaperonin to close slightly with a ∼45° counterclockwise rotation of the apical domain. The subsequent ATP hydrolysis drives each subunit to rock toward the folding chamber and to close the lid completely. These motions are attributable to the local interactions of specific active site residues with the nucleotide, the tight couplings between the apical and intermediate domains within the subunit, and the aligned interactions between two subunits across the rings. This mechanism of structural changes in response to ATP is entirely different from those found in group I chaperonins.

PubMed: 21565698
DOI: 10.1016/j.str.2011.03.005

実験手法

ELECTRON MICROSCOPY (8 Å)