8QYC
Zorya anti-bacteriophage defense system ZorD in complex with ATP-gamma-S
Summary for 8QYC
Entry DOI | 10.2210/pdb8qyc/pdb |
EMDB information | 18750 |
Descriptor | DEAD/DEAH box helicase, PHOSPHOTHIOPHOSPHORIC ACID-ADENYLATE ESTER (2 entities in total) |
Functional Keywords | nuclease, antiviral protein |
Biological source | Escherichia coli |
Total number of polymer chains | 1 |
Total formula weight | 123403.29 |
Authors | Hu, H.,Taylor, N.M.I. (deposition date: 2023-10-25, release date: 2024-11-06, Last modification date: 2025-04-09) |
Primary citation | Hu, H.,Popp, P.F.,Hughes, T.C.D.,Roa-Eguiara, A.,Rutbeek, N.R.,Martin, F.J.O.,Hendriks, I.A.,Payne, L.J.,Yan, Y.,Humolli, D.,Klein-Sousa, V.,Songailiene, I.,Wang, Y.,Nielsen, M.L.,Berry, R.M.,Harms, A.,Erhardt, M.,Jackson, S.A.,Taylor, N.M.I. Structure and mechanism of the Zorya anti-phage defence system. Nature, 639:1093-1101, 2025 Cited by PubMed Abstract: Zorya is a recently identified and widely distributed bacterial immune system that protects bacteria from viral (phage) infections. Three Zorya subtypes have been identified, each containing predicted membrane-embedded ZorA-ZorB (ZorAB) complexes paired with soluble subunits that differ among Zorya subtypes, notably ZorC and ZorD in type I Zorya systems. Here we investigate the molecular basis of Zorya defence using cryo-electron microscopy, mutagenesis, fluorescence microscopy, proteomics and functional studies. We present cryo-electron microscopy structures of ZorAB and show that it shares stoichiometry and features of other 5:2 inner membrane ion-driven rotary motors. The ZorAB complex contains a dimeric ZorB peptidoglycan-binding domain and a pentameric α-helical coiled-coil tail made of ZorA that projects approximately 70 nm into the cytoplasm. We also characterize the structure and function of the soluble Zorya components ZorC and ZorD, finding that they have DNA-binding and nuclease activity, respectively. Comprehensive functional and mutational analyses demonstrate that all Zorya components work in concert to protect bacterial cells against invading phages. We provide evidence that ZorAB operates as a proton-driven motor that becomes activated after sensing of phage invasion. Subsequently, ZorAB transfers the phage invasion signal through the ZorA cytoplasmic tail to recruit and activate the soluble ZorC and ZorD effectors, which facilitate the degradation of the phage DNA. In summary, our study elucidates the foundational mechanisms of Zorya function as an anti-phage defence system. PubMed: 39662505DOI: 10.1038/s41586-024-08493-8 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.75 Å) |
Structure validation
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