5WTK
Crystal structure of RNP complex
5WTK の概要
| エントリーDOI | 10.2210/pdb5wtk/pdb |
| 関連するPDBエントリー | 5WTJ |
| 分子名称 | CRISPR-associated endoribonuclease C2c2, RNA (58-MER) (3 entities in total) |
| 機能のキーワード | hydrolase-rna complex, hydrolase/rna |
| 由来する生物種 | Leptotrichia shahii (strain DSM 19757 / CCUG 47503 / CIP 107916 / JCM 16776 / LB37) 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 186157.72 |
| 構造登録者 | |
| 主引用文献 | Liu, L.,Li, X.,Wang, J.,Wang, M.,Chen, P.,Yin, M.,Li, J.,Sheng, G.,Wang, Y. Two Distant Catalytic Sites Are Responsible for C2c2 RNase Activities Cell, 168:121-134.e12, 2017 Cited by PubMed Abstract: C2c2, the effector of type VI CRISPR-Cas systems, has two RNase activities-one for cutting its RNA target and the other for processing the CRISPR RNA (crRNA). Here, we report the structures of Leptotrichia shahii C2c2 in its crRNA-free and crRNA-bound states. While C2c2 has a bilobed structure reminiscent of all other Class 2 effectors, it also exhibits different structural characteristics. It contains the REC lobe with a Helical-1 domain and the NUC lobe with two HEPN domains. The two RNase catalytic pockets responsible for cleaving pre-crRNA and target RNA are independently located on Helical-1 and HEPN domains, respectively. crRNA binding induces significant conformational changes that are likely to stabilize crRNA binding and facilitate target RNA recognition. These structures provide important insights into the molecular mechanism of dual RNase activities of C2c2 and establish a framework for its future engineering as a RNA editing tool. PubMed: 28086085DOI: 10.1016/j.cell.2016.12.031 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.651 Å) |
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