8HI1
Streptococcus thermophilus Cas1-Cas2- prespacer ternary complex
8HI1 の概要
エントリーDOI | 10.2210/pdb8hi1/pdb |
EMDBエントリー | 34809 |
分子名称 | CRISPR-associated endonuclease Cas1, Type I-E CRISPR-associated endoribonuclease Cas2, DNA (26-MER), ... (4 entities in total) |
機能のキーワード | crispr, cas, adaptation, immune system |
由来する生物種 | Streptococcus thermophilus DGCC 7710 詳細 |
タンパク質・核酸の鎖数 | 8 |
化学式量合計 | 193530.10 |
構造登録者 | |
主引用文献 | Tang, D.,Jia, T.,Luo, Y.,Mou, B.,Cheng, J.,Qi, S.,Yao, S.,Su, Z.,Yu, Y.,Chen, Q. DnaQ mediates directional spacer acquisition in the CRISPR-Cas system by a time-dependent mechanism. Innovation (N Y), 4:100495-100495, 2023 Cited by PubMed Abstract: In the spacer acquisition stage of CRISPR-Cas immunity, spacer orientation and protospacer adjacent motif (PAM) removal are two prerequisites for functional spacer integration. Cas4 has been implicated in both processing the prespacer and determining the spacer orientation. In Cas4-lacking systems, host 3'-5' DnaQ family exonucleases were recently reported to play a Cas4-like role. However, the molecular details of DnaQ functions remain elusive. Here, we characterized the spacer acquisition of the adaptation module of the type I-E system, in which a DnaQ domain naturally fuses with Cas2. We presented X-ray crystal structures and cryo-electron microscopy structures of this adaptation module. Our biochemical data showed that DnaQ trimmed PAM-containing and PAM-deficient overhangs with different efficiencies. Based on these results, we proposed a time-dependent model for DnaQ-mediated spacer acquisition to elucidate PAM removal and spacer orientation determination in Cas4-lacking CRISPR-Cas systems. PubMed: 37663930DOI: 10.1016/j.xinn.2023.100495 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (3.09 Å) |
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