8Q86
Trimer of the dimeric SaPI2 Stl transcriptional regulator
Summary for 8Q86
| Entry DOI | 10.2210/pdb8q86/pdb |
| EMDB information | 18248 |
| Descriptor | Helix-turn-helix XRE family protein (2 entities in total) |
| Functional Keywords | transcriptional regulator, stl, staphylococcus aureus pathogenicity island, sapi, sapi2, phage-inducible chromosomal island, pici, picis, transcriptional repressor, transcription regulator, repressor, dna-binding, dna binding protein |
| Biological source | Staphylococcus aureus |
| Total number of polymer chains | 8 |
| Total formula weight | 217516.50 |
| Authors | |
| Primary citation | Debiasi-Anders, G.,Qiao, C.,Salim, A.,Li, N.,Mir-Sanchis, I. Phage parasites targeting phage homologous recombinases provide antiviral immunity. Nat Commun, 16:1889-1889, 2025 Cited by PubMed Abstract: Bacteria often carry multiple genes encoding anti-phage defense systems, clustered in defense islands and phage satellites. Various unrelated anti-phage defense systems target phage-encoded homologous recombinases (HRs) through unclear mechanisms. Here, we show that the phage satellite SaPI2, which does not encode orthodox anti-phage defense systems, provides antiviral immunity mediated by Stl2, the SaPI2-encoded transcriptional repressor. Stl2 targets and inhibits phage-encoded HRs, including Sak and Sak4, two HRs from the Rad52-like and Rad51-like superfamilies. Remarkably, apo Stl2 forms a collar of dimers oligomerizing as closed rings and as filaments, mimicking the quaternary structure of its targets. Stl2 decorates both Sak rings and Sak4 filaments. The oligomerization of Stl2 as a collar of dimers is necessary for its inhibitory activity both in vitro and in vivo. Our results shed light on the mechanisms underlying antiviral immunity against phages carrying divergent HRs. PubMed: 39987160DOI: 10.1038/s41467-025-57156-3 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.69 Å) |
Structure validation
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