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6TUN

Helicase domain complex

6TUN の概要
エントリーDOI10.2210/pdb6tun/pdb
分子名称General transcription and DNA repair factor IIH helicase subunit XPD, CDK-activating kinase assembly factor MAT1, CHLORIDE ION, ... (4 entities in total)
機能のキーワードhelicase, dna-repair, transcription, cell cylcle, nuclear protein
由来する生物種Homo sapiens (Human)
詳細
タンパク質・核酸の鎖数4
化学式量合計63761.97
構造登録者
Sauer, F.,Kisker, C. (登録日: 2020-01-07, 公開日: 2020-11-11, 最終更新日: 2024-05-15)
主引用文献Peissert, S.,Sauer, F.,Grabarczyk, D.B.,Braun, C.,Sander, G.,Poterszman, A.,Egly, J.M.,Kuper, J.,Kisker, C.
In TFIIH the Arch domain of XPD is mechanistically essential for transcription and DNA repair.
Nat Commun, 11:1667-1667, 2020
Cited by
PubMed Abstract: The XPD helicase is a central component of the general transcription factor TFIIH which plays major roles in transcription and nucleotide excision repair (NER). Here we present the high-resolution crystal structure of the Arch domain of XPD with its interaction partner MAT1, a central component of the CDK activating kinase complex. The analysis of the interface led to the identification of amino acid residues that are crucial for the MAT1-XPD interaction. More importantly, mutagenesis of the Arch domain revealed that these residues are essential for the regulation of (i) NER activity by either impairing XPD helicase activity or the interaction of XPD with XPG; (ii) the phosphorylation of the RNA polymerase II and RNA synthesis. Our results reveal how MAT1 shields these functionally important residues thereby providing insights into how XPD is regulated by MAT1 and defining the Arch domain as a major mechanistic player within the XPD scaffold.
PubMed: 32245994
DOI: 10.1038/s41467-020-15241-9
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.07 Å)
構造検証レポート
Validation report summary of 6tun
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2026-02-04に公開中

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