6TUN
Helicase domain complex
6TUN の概要
| エントリーDOI | 10.2210/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 | |
| 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: 32245994DOI: 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) |
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