2GXB
Crystal Structure of The Za Domain bound to Z-RNA
2GXB の概要
エントリーDOI | 10.2210/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 | |
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: 17437712DOI: 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) |
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