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8Q86

Trimer of the dimeric SaPI2 Stl transcriptional regulator

8Q86 の概要
エントリーDOI10.2210/pdb8q86/pdb
EMDBエントリー18248
分子名称Helix-turn-helix XRE family protein (2 entities in total)
機能のキーワード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
由来する生物種Staphylococcus aureus
タンパク質・核酸の鎖数8
化学式量合計217516.50
構造登録者
Qiao, C.,Debiasi-Anders, G.,Mir-Sanchis, I. (登録日: 2023-08-18, 公開日: 2025-03-05)
主引用文献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: 39987160
DOI: 10.1038/s41467-025-57156-3
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.69 Å)
構造検証レポート
Validation report summary of 8q86
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-22に公開中

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