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6NY2

CasX-gRNA-DNA(45bp) state I

6E79」から置き換えられました
6NY2 の概要
エントリーDOI10.2210/pdb6ny2/pdb
EMDBエントリー8980 8994 8996
分子名称DNA target strand, DNA Non-target strand, CasX, ... (4 entities in total)
機能のキーワードcasx, sgrna, target dna, crispr, rna binding protein-rna-dna complex, rna binding protein/rna/dna
由来する生物種Deltaproteobacteria bacterium
詳細
タンパク質・核酸の鎖数4
化学式量合計174931.92
構造登録者
Liu, J.J.,Orlova, N.,Nogales, E.,Doudna, J.A. (登録日: 2019-02-10, 公開日: 2019-02-27, 最終更新日: 2019-12-25)
主引用文献Liu, J.J.,Orlova, N.,Oakes, B.L.,Ma, E.,Spinner, H.B.,Baney, K.L.M.,Chuck, J.,Tan, D.,Knott, G.J.,Harrington, L.B.,Al-Shayeb, B.,Wagner, A.,Brotzmann, J.,Staahl, B.T.,Taylor, K.L.,Desmarais, J.,Nogales, E.,Doudna, J.A.
CasX enzymes comprise a distinct family of RNA-guided genome editors.
Nature, 566:218-223, 2019
Cited by
PubMed Abstract: The RNA-guided CRISPR-associated (Cas) proteins Cas9 and Cas12a provide adaptive immunity against invading nucleic acids, and function as powerful tools for genome editing in a wide range of organisms. Here we reveal the underlying mechanisms of a third, fundamentally distinct RNA-guided genome-editing platform named CRISPR-CasX, which uses unique structures for programmable double-stranded DNA binding and cleavage. Biochemical and in vivo data demonstrate that CasX is active for Escherichia coli and human genome modification. Eight cryo-electron microscopy structures of CasX in different states of assembly with its guide RNA and double-stranded DNA substrates reveal an extensive RNA scaffold and a domain required for DNA unwinding. These data demonstrate how CasX activity arose through convergent evolution to establish an enzyme family that is functionally separate from both Cas9 and Cas12a.
PubMed: 30718774
DOI: 10.1038/s41586-019-0908-x
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.2 Å)
構造検証レポート
Validation report summary of 6ny2
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2024-10-30に公開中

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