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6J9M

NmeBH+AcrIIC2

6J9M の概要
エントリーDOI10.2210/pdb6j9m/pdb
分子名称CRISPR-associated endonuclease Cas9, AcrIIC2 (3 entities in total)
機能のキーワードacriic2, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
由来する生物種Neisseria meningitidis
詳細
タンパク質・核酸の鎖数6
化学式量合計74141.73
構造登録者
Zhu, Y.L.,Gao, A.,Serganov, A.,Gao, P. (登録日: 2019-01-23, 公開日: 2019-03-06, 最終更新日: 2023-11-22)
主引用文献Zhu, Y.,Gao, A.,Zhan, Q.,Wang, Y.,Feng, H.,Liu, S.,Gao, G.,Serganov, A.,Gao, P.
Diverse Mechanisms of CRISPR-Cas9 Inhibition by Type IIC Anti-CRISPR Proteins.
Mol. Cell, 74:296-309.e7, 2019
Cited by
PubMed Abstract: Anti-CRISPR proteins (Acrs) targeting CRISPR-Cas9 systems represent natural "off switches" for Cas9-based applications. Recently, AcrIIC1, AcrIIC2, and AcrIIC3 proteins were found to inhibit Neisseria meningitidis Cas9 (NmeCas9) activity in bacterial and human cells. Here we report biochemical and structural data that suggest molecular mechanisms of AcrIIC2- and AcrIIC3-mediated Cas9 inhibition. AcrIIC2 dimer interacts with the bridge helix of Cas9, interferes with RNA binding, and prevents DNA loading into Cas9. AcrIIC3 blocks the DNA loading step through binding to a non-conserved surface of the HNH domain of Cas9. AcrIIC3 also forms additional interactions with the REC lobe of Cas9 and induces the dimerization of the AcrIIC3-Cas9 complex. While AcrIIC2 targets Cas9 orthologs from different subtypes, albeit with different efficiency, AcrIIC3 specifically inhibits NmeCas9. Structure-guided changes in NmeCas9 orthologs convert them into anti-CRISPR-sensitive proteins. Our studies provide insights into anti-CRISPR-mediated suppression mechanisms and guidelines for designing regulatory tools in Cas9-based applications.
PubMed: 30850331
DOI: 10.1016/j.molcel.2019.01.038
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.394 Å)
構造検証レポート
Validation report summary of 6j9m
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2024-11-13に公開中

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