6SKO

Cryo-EM Structure of the Fork Protection Complex Bound to CMG at a Replication Fork - conformation 2 MCM CTD:ssDNA

6SKO の概要

• エントリーDOI: 10.2210/pdb6sko/pdb
• EMDBエントリー: 10230
• 分子名称: DNA replication licensing factor MCM6, DNA replication licensing factor MCM7, DNA replication licensing factor MCM2, ... (9 entities in total)
• 機能のキーワード: protein-dna complex, replisome, aaa+ helicase, cmg, gins, fork dna, mcm, fork protection complex, cip-box, replication
• 由来する生物種: Saccharomyces cerevisiae (strain ATCC 204508 / S288c); 詳細
• タンパク質・核酸の鎖数: 7
• 化学式量合計: 635418.58

構造登録者

Yeeles, J.,Baretic, D.,Jenkyn-Bedford, M. (登録日: 2019-08-16, 公開日: 2020-05-06, 最終更新日: 2024-05-22)

主引用文献

Baretic, D.,Jenkyn-Bedford, M.,Aria, V.,Cannone, G.,Skehel, M.,Yeeles, J.T.P.
Cryo-EM Structure of the Fork Protection Complex Bound to CMG at a Replication Fork.
Mol.Cell, 78:926-940.e13, 2020

PubMed Abstract: The eukaryotic replisome, organized around the Cdc45-MCM-GINS (CMG) helicase, orchestrates chromosome replication. Multiple factors associate directly with CMG, including Ctf4 and the heterotrimeric fork protection complex (Csm3/Tof1 and Mrc1), which has important roles including aiding normal replication rates and stabilizing stalled forks. How these proteins interface with CMG to execute these functions is poorly understood. Here we present 3 to 3.5 Å resolution electron cryomicroscopy (cryo-EM) structures comprising CMG, Ctf4, and the fork protection complex at a replication fork. The structures provide high-resolution views of CMG-DNA interactions, revealing a mechanism for strand separation, and show Csm3/Tof1 "grip" duplex DNA ahead of CMG via a network of interactions important for efficient replication fork pausing. Although Mrc1 was not resolved in our structures, we determine its topology in the replisome by cross-linking mass spectrometry. Collectively, our work reveals how four highly conserved replisome components collaborate with CMG to facilitate replisome progression and maintain genome stability.

PubMed: 32369734
DOI: 10.1016/j.molcel.2020.04.012

実験手法

ELECTRON MICROSCOPY (3.4 Å)