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5ANR

Structure of a human 4E-T - DDX6 - CNOT1 complex

5ANR の概要
エントリーDOI10.2210/pdb5anr/pdb
分子名称CCR4-NOT TRANSCRIPTION COMPLEX SUBUNIT 1, PROBABLE ATP-DEPENDENT RNA HELICASE DDX6, EUKARYOTIC TRANSLATION INITIATION FACTOR 4E TRANSPORTER, ... (4 entities in total)
機能のキーワードrna binding protein
由来する生物種HOMO SAPIENS (HUMAN)
詳細
細胞内の位置Cytoplasm, P-body : A5YKK6 P26196
Cytoplasm : Q9NRA8
タンパク質・核酸の鎖数3
化学式量合計77976.94
構造登録者
Basquin, J.,Oezguer, S.,Conti, E. (登録日: 2015-09-08, 公開日: 2015-10-21, 最終更新日: 2024-01-10)
主引用文献Ozgur, S.,Basquin, J.,Kamenska, A.,Filipowicz, W.,Standart, N.,Conti, E.
Structure of a Human 4E-T/Ddx6/Cnot1 Complex Reveals the Different Interplay of Ddx6-Binding Proteins with the Ccr4-not Complex.
Cell Rep., 13:703-, 2015
Cited by
PubMed Abstract: The DEAD-box protein DDX6 is a central component of translational repression mechanisms in maternal mRNA storage in oocytes and microRNA-mediated silencing in somatic cells. DDX6 interacts with the CCR4-NOT complex and functions in concert with several post-transcriptional regulators, including Edc3, Pat1, and 4E-T. We show that the conserved CUP-homology domain (CHD) of human 4E-T interacts directly with DDX6 in both the presence and absence of the central MIF4G domain of CNOT1. The 2.1-Å resolution structure of the corresponding ternary complex reveals how 4E-T CHD wraps around the RecA2 domain of DDX6 and contacts CNOT1. Although 4E-T CHD lacks recognizable sequence similarity with Edc3 or Pat1, it shares the same DDX6-binding surface. In contrast to 4E-T, however, the Edc3 and Pat1 FDF motifs dissociate from DDX6 upon CNOT1 MIF4G binding in vitro. The results underscore the presence of a complex network of simultaneous and/or mutually exclusive interactions in DDX6-mediated repression.
PubMed: 26489469
DOI: 10.1016/J.CELREP.2015.09.033
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.102 Å)
構造検証レポート
Validation report summary of 5anr
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2026-04-22に公開中

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