8RFJ
DNA bound type IV-A1 CRISPR effector complex with the DinG helicase from P. oleovorans
8RFJ の概要
| エントリーDOI | 10.2210/pdb8rfj/pdb |
| EMDBエントリー | 19125 |
| 分子名称 | CRISPR type AFERR-associated protein Csf2, CRISPR type AFERR-associated protein Csf3, CRISPR type AFERR-associated protein Csf1, ... (9 entities in total) |
| 機能のキーワード | crispr, crrna, dna binding, type iv crispr-cas, crispri, nuclease deficient, gene regulation |
| 由来する生物種 | Pseudomonas oleovorans 詳細 |
| タンパク質・核酸の鎖数 | 12 |
| 化学式量合計 | 398589.20 |
| 構造登録者 | |
| 主引用文献 | Cepaite, R.,Klein, N.,Miksys, A.,Camara-Wilpert, S.,Ragozius, V.,Benz, F.,Skorupskaite, A.,Becker, H.,Zvejyte, G.,Steube, N.,Hochberg, G.K.A.,Randau, L.,Pinilla-Redondo, R.,Malinauskaite, L.,Pausch, P. Structural variation of types IV-A1- and IV-A3-mediated CRISPR interference. Nat Commun, 15:9306-9306, 2024 Cited by PubMed Abstract: CRISPR-Cas mediated DNA-interference typically relies on sequence-specific binding and nucleolytic degradation of foreign genetic material. Type IV-A CRISPR-Cas systems diverge from this general mechanism, using a nuclease-independent interference pathway to suppress gene expression for gene regulation and plasmid competition. To understand how the type IV-A system associated effector complex achieves this interference, we determine cryo-EM structures of two evolutionarily distinct type IV-A complexes (types IV-A1 and IV-A3) bound to cognate DNA-targets in the presence and absence of the type IV-A signature DinG effector helicase. The structures reveal how the effector complexes recognize the protospacer adjacent motif and target-strand DNA to form an R-loop structure. Additionally, we reveal differences between types IV-A1 and IV-A3 in DNA interactions and structural motifs that allow for in trans recruitment of DinG. Our study provides a detailed view of type IV-A mediated DNA-interference and presents a structural foundation for engineering type IV-A-based genome editing tools. PubMed: 39468082DOI: 10.1038/s41467-024-53778-1 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.18 Å) |
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