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2GXB

Crystal Structure of The Za Domain bound to Z-RNA

2GXB の概要
エントリーDOI10.2210/pdb2gxb/pdb
関連するPDBエントリー1QBJ 1QJP 1XMK
分子名称5'-R(P*(DU)P*CP*GP*CP*GP*CP*G)-3', Double-stranded RNA-specific adenosine deaminase, SODIUM ION, ... (4 entities in total)
機能のキーワードz-rna, za, adar1, rna editing, protein-rna complex, hydrolase-rna complex, hydrolase/rna
由来する生物種Homo sapiens (human)
細胞内の位置Cytoplasm: P55265
タンパク質・核酸の鎖数4
化学式量合計19092.78
構造登録者
Athanasiadis, A.,Placido, D.,Rich, A. (登録日: 2006-05-08, 公開日: 2007-05-01, 最終更新日: 2023-08-30)
主引用文献Placido, D.,Brown, B.A.,Lowenhaupt, K.,Rich, A.,Athanasiadis, A.
A Left-Handed RNA Double Helix Bound by the Zalpha Domain of the RNA-Editing Enzyme ADAR1.
Structure, 15:395-404, 2007
Cited by
PubMed Abstract: The A form RNA double helix can be transformed to a left-handed helix, called Z-RNA. Currently, little is known about the detailed structural features of Z-RNA or its involvement in cellular processes. The discovery that certain interferon-response proteins have domains that can stabilize Z-RNA as well as Z-DNA opens the way for the study of Z-RNA. Here, we present the 2.25 A crystal structure of the Zalpha domain of the RNA-editing enzyme ADAR1 (double-stranded RNA adenosine deaminase) complexed to a dUr(CG)(3) duplex RNA. The Z-RNA helix is associated with a unique solvent pattern that distinguishes it from the otherwise similar conformation of Z-DNA. Based on the structure, we propose a model suggesting how differences in solvation lead to two types of Z-RNA structures. The interaction of Zalpha with Z-RNA demonstrates how the interferon-induced isoform of ADAR1 could be targeted toward selected dsRNAs containing purine-pyrimidine repeats, possibly of viral origin.
PubMed: 17437712
DOI: 10.1016/j.str.2007.03.001
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.25 Å)
構造検証レポート
Validation report summary of 2gxb
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2024-11-06に公開中

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