4AB3

ATP-triggered molecular mechanics of the chaperonin GroEL

4AB3 の概要

• エントリーDOI: 10.2210/pdb4ab3/pdb
• 関連するPDBエントリー: 1AON 1DK7 1DKD 1FY9 1FYA 1GR5 1GRL 1GRU 1J4Z 1JON 1KID 1KP8 1KPO 1LA1 1MNF 1OEL 1PCQ 1PF9 1SS8 1SVT 1SX3 1SX4 1XCK 2C7C 2C7D 2C7E 2CGT 2YEY 4AAQ 4AAR 4AAS 4AAU 4AB2
• EMDBエントリー: 2003
• 分子名称: 60 KDA CHAPERONIN, PHOSPHATE ION, MAGNESIUM ION, ... (4 entities in total)
• 機能のキーワード: chaperone
• 由来する生物種: ESCHERICHIA COLI
• 細胞内の位置: Cytoplasm : P0A6F5
• タンパク質・核酸の鎖数: 14
• 化学式量合計: 811638.24

構造登録者

Clare, D.K.,Vasishtan, D.,Stagg, S.,Quispe, J.,Farr, G.W.,Topf, M.,Horwich, A.L.,Saibil, H.R. (登録日: 2011-12-06, 公開日: 2012-12-12, 最終更新日: 2024-05-08)

主引用文献

Clare, D.K.,Vasishtan, D.,Stagg, S.,Quispe, J.,Farr, G.W.,Topf, M.,Horwich, A.L.,Saibil, H.R.
ATP-Triggered Conformational Changes Delineate Substrate-Binding and -Folding Mechanics of the Groel Chaperonin.
Cell(Cambridge,Mass.), 149:113-, 2012

PubMed Abstract: The chaperonin GroEL assists the folding of nascent or stress-denatured polypeptides by actions of binding and encapsulation. ATP binding initiates a series of conformational changes triggering the association of the cochaperonin GroES, followed by further large movements that eject the substrate polypeptide from hydrophobic binding sites into a GroES-capped, hydrophilic folding chamber. We used cryo-electron microscopy, statistical analysis, and flexible fitting to resolve a set of distinct GroEL-ATP conformations that can be ordered into a trajectory of domain rotation and elevation. The initial conformations are likely to be the ones that capture polypeptide substrate. Then the binding domains extend radially to separate from each other but maintain their binding surfaces facing the cavity, potentially exerting mechanical force upon kinetically trapped, misfolded substrates. The extended conformation also provides a potential docking site for GroES, to trigger the final, 100° domain rotation constituting the "power stroke" that ejects substrate into the folding chamber.

PubMed: 22445172
DOI: 10.1016/J.CELL.2012.02.047

実験手法

ELECTRON MICROSCOPY (8.5 Å)