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9E8Z

4-component structure of retron Ec83

Summary for 9E8Z
Entry DOI10.2210/pdb9e8z/pdb
EMDB information47737
DescriptorRetron Ec83 probable ATPase, Retron Ec83 putative HNH endonuclease, Retron Ec83 reverse transcriptase, ... (7 entities in total)
Functional Keywordsatpase, hnh-endonuclease, retron, msdna, antiviral protein
Biological sourceEscherichia coli
More
Total number of polymer chains9
Total formula weight381979.35
Authors
Rish, A.D.,Wang, C.,Fu, T.M. (deposition date: 2024-11-06, release date: 2025-07-02, Last modification date: 2025-09-03)
Primary citationWang, C.,Rish, A.D.,Armbruster, E.G.,Xie, J.,Loveland, A.B.,Shen, Z.,Gu, B.,Korostelev, A.A.,Pogliano, J.,Fu, T.M.
Disassembly activates Retron-Septu for antiphage defense.
Science, 389:eadv3344-eadv3344, 2025
Cited by
PubMed Abstract: Retrons are antiphage defense systems that produce multicopy single-stranded DNA (msDNA) and hold promises for genome engineering. However, the mechanisms of defense remain unclear. The Retron-Septu system uniquely integrates retron and Septu antiphage defenses. Cryo-electron microscopy structures reveal asymmetric nucleoprotein complexes comprising a reverse transcriptase (RT), msDNA (a hybrid of msdDNA and msrRNA), and two PtuAB copies. msdDNA and msrRNA are essential for assembling this complex, with msrRNA adopting a conserved lariat-like structure that regulates reverse transcription. Notably, the assembled Retron-Septu complex is inactive, with msdDNA occupying the PtuA DNA-binding site. Activation occurs upon disassembly, releasing PtuAB, which degrades single-stranded DNA to restrict phage replication. This "arrest-and-release" mechanism underscores the dynamic regulatory roles of msDNA, advancing our understanding of antiphage defense strategies.
PubMed: 40504952
DOI: 10.1126/science.adv3344
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.47 Å)
Structure validation

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