6NY2 の概要
エントリーDOI | 10.2210/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 | |
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: 30718774DOI: 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) |
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