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9CEU

Spizellomyces punctatus Fanzor (SpuFz) State 1

Summary for 9CEU
Entry DOI10.2210/pdb9ceu/pdb
EMDB information45519
DescriptorDNA (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 (5'-D(P*CP*CP*TP*AP*TP*AP*GP*AP*TP*AP*TP*GP*CP*CP*CP*GP*GP*GP*TP*AP*CP*CP*G)-3'), ... (5 entities in total)
Functional Keywordsfanzor, eukaryotic, rna-guided, nuclease, gene editing, rna binding protein-rna-dna complex, rna binding protein/rna/dna
Biological sourceEscherichia coli K-12
More
Total number of polymer chains4
Total formula weight182098.91
Authors
Xu, P.,Saito, M.,Zhang, F. (deposition date: 2024-06-27, release date: 2024-09-11, Last modification date: 2024-10-02)
Primary citationXu, 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
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.29 Å)
Structure validation

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