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9CEW

Spizellomyces punctatus Fanzor (SpuFz) State 3

9CEW の概要
エントリーDOI10.2210/pdb9cew/pdb
EMDBエントリー45521
分子名称DNA (5'-D(P*CP*GP*GP*TP*AP*CP*CP*CP*GP*GP*GP*CP*AP*TP*A)-3'), Maltose/maltodextrin-binding periplasmic protein,Spizellomyces punctatus Fanzor 1, DNA (29-MER), ... (8 entities in total)
機能のキーワードfanzor, eukaryotic, rna-guided, nuclease, gene editing, rna binding protein-rna-dna complex, rna binding protein/rna/dna
由来する生物種Escherichia coli K-12
詳細
タンパク質・核酸の鎖数6
化学式量合計196257.79
構造登録者
Xu, P.,Saito, M.,Zhang, F. (登録日: 2024-06-27, 公開日: 2024-09-11, 最終更新日: 2024-10-02)
主引用文献Xu, P.,Saito, M.,Faure, G.,Maguire, S.,Chau-Duy-Tam Vo, S.,Wilkinson, M.E.,Kuang, H.,Wang, B.,Rice, W.J.,Macrae, R.K.,Zhang, F.
Structural insights into the diversity and DNA cleavage mechanism of Fanzor.
Cell, 187:5238-5252.e20, 2024
Cited by
PubMed Abstract: Fanzor (Fz) is an ωRNA-guided endonuclease extensively found throughout the eukaryotic domain with unique gene editing potential. Here, we describe the structures of Fzs from three different organisms. We find that Fzs share a common ωRNA interaction interface, regardless of the length of the ωRNA, which varies considerably across species. The analysis also reveals Fz's mode of DNA recognition and unwinding capabilities as well as the presence of a non-canonical catalytic site. The structures demonstrate how protein conformations of Fz shift to allow the binding of double-stranded DNA to the active site within the R-loop. Mechanistically, examination of structures in different states shows that the conformation of the lid loop on the RuvC domain is controlled by the formation of the guide/DNA heteroduplex, regulating the activation of nuclease and DNA double-stranded displacement at the single cleavage site. Our findings clarify the mechanism of Fz, establishing a foundation for engineering efforts.
PubMed: 39208796
DOI: 10.1016/j.cell.2024.07.050
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.88 Å)
構造検証レポート
Validation report summary of 9cew
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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