7VOI

Structure of the human CNOT1(MIF4G)-CNOT6L-CNOT7 complex

7VOI の概要

• エントリーDOI: 10.2210/pdb7voi/pdb
• 分子名称: CCR4-NOT transcription complex subunit 7, CCR4-NOT transcription complex subunit 1, CCR4-NOT transcription complex subunit 6-like (3 entities in total)
• 機能のキーワード: ccr4-not complex mrna degradation, rna binding protein, hydrolase
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 122481.26

構造登録者

Bartlam, M.,Zhang, Q. (登録日: 2021-10-13, 公開日: 2022-06-01, 最終更新日: 2023-11-29)

主引用文献

Zhang, Q.,Pavanello, L.,Potapov, A.,Bartlam, M.,Winkler, G.S.
Structure of the human Ccr4-Not nuclease module using X-ray crystallography and electron paramagnetic resonance spectroscopy distance measurements.
Protein Sci., 31:758-764, 2022

PubMed Abstract: Regulated degradation of mature, cytoplasmic mRNA is a key step in eukaryotic gene regulation. This process is typically initiated by the recruitment of deadenylase enzymes by cis-acting elements in the 3' untranslated region resulting in the shortening and removal of the 3' poly(A) tail of the target mRNA. The Ccr4-Not complex, a major eukaryotic deadenylase, contains two exoribonuclease subunits with selectivity toward poly(A): Caf1 and Ccr4. The Caf1 deadenylase subunit binds the MIF4G domain of the large subunit CNOT1 (Not1) that is the scaffold of the complex. The Ccr4 nuclease is connected to the complex via its leucine-rich repeat (LRR) domain, which binds Caf1, whereas the catalytic activity of Ccr4 is provided by its EEP domain. While the relative positions of the MIF4G domain of CNOT1, the Caf1 subunit, and the LRR domain of Ccr4 are clearly defined in current models, the position of the EEP nuclease domain of Ccr4 is ambiguous. Here, we use X-ray crystallography, the AlphaFold resource of predicted protein structures, and pulse electron paramagnetic resonance spectroscopy to determine and validate the position of the EEP nuclease domain of Ccr4 resulting in an improved model of the human Ccr4-Not nuclease module.

PubMed: 34923703
DOI: 10.1002/pro.4262

実験手法

X-RAY DIFFRACTION (4.38 Å)