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5YFG

SOLUTION STRUCTURE OF HUMAN MOG1

5YFG の概要
エントリーDOI10.2210/pdb5yfg/pdb
NMR情報BMRB: 36117
分子名称Ran guanine nucleotide release factor (1 entity in total)
機能のキーワードcentral beta sheet, alternative splicing, cytoplasm, guanine-nucleotide releasing factor, nucleus, protein transport
由来する生物種Homo sapiens (Human)
細胞内の位置Nucleus : Q9HD47
タンパク質・核酸の鎖数1
化学式量合計21523.15
構造登録者
Hu, Q.,Liu, Y.,Bao, X.,Liu, H. (登録日: 2017-09-21, 公開日: 2017-11-01, 最終更新日: 2024-05-15)
主引用文献Bao, X.,Liu, H.,Liu, X.,Ruan, K.,Zhang, Y.,Zhang, Z.,Hu, Q.,Liu, Y.,Akram, S.,Zhang, J.,Gong, Q.,Wang, W.,Yuan, X.,Li, J.,Zhao, L.,Dou, Z.,Tian, R.,Yao, X.,Wu, J.,Shi, Y.
Mitosis-specific acetylation tunes Ran effector binding for chromosome segregation
J Mol Cell Biol, 10:18-32, 2018
Cited by
PubMed Abstract: Stable transmission of genetic information during cell division requires faithful mitotic spindle assembly and chromosome segregation. The Ran GTPase plays a key role in mitotic spindle assembly. However, how the generation of a chemical gradient of Ran-GTP at the spindle is coupled to mitotic post-translational modifications has never been characterized. Here, we solved the complex structure of Ran with the nucleotide release factor Mog1 and delineated a novel mitosis-specific acetylation-regulated Ran-Mog1 interaction during chromosome segregation. Our structure-guided functional analyses revealed that Mog1 competes with RCC1 for Ran binding in a GTP/GDP-dependent manner. Biochemical characterization demonstrated that Mog1-bound Ran prevents RCC1 binding and subsequent GTP loading. Surprisingly, Ran is a bona fide substrate of TIP60, and the acetylation of Lys134 by TIP60 liberates Mog1 from Ran binding during mitosis. Importantly, this acetylation-elicited switch of Ran binding to RCC1 promotes high level of Ran-GTP, which is essential for chromosome alignment. These results establish a previously uncharacterized regulatory mechanism in which TIP60 provides a homeostatic control of Ran-GTP level by tuning Ran effector binding for chromosome segregation in mitosis.
PubMed: 29040603
DOI: 10.1093/jmcb/mjx045
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 5yfg
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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