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9O4A

Ec83 Retron PtuAB mutant complex

Summary for 9O4A
Entry DOI10.2210/pdb9o4a/pdb
Related9E8Z 9E90 9E91
EMDB information70091
DescriptorRetron Ec83 probable ATPase, Retron Ec83 putative HNH endonuclease, ADENOSINE-5'-TRIPHOSPHATE, ... (4 entities in total)
Functional Keywordsretron, ptua, ptub, atpase, hnh nuclease, immune system
Biological sourceEscherichia coli
More
Total number of polymer chains3
Total formula weight154577.75
Authors
Wang, C.,Rish, A.,Fu, T.M. (deposition date: 2025-04-08, release date: 2025-07-02)
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, :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 (2.8 Å)
Structure validation

238268

數據於2025-07-02公開中

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