9BKQ

Structure of penguinpox cGAMP PDE in apo and post reaction states

これはPDB形式変換不可エントリーです。

9BKQ の概要

• エントリーDOI: 10.2210/pdb9bkq/pdb
• 分子名称: Penguinpox cGAMP PDE, 9-{3-O-[(S)-thiophosphono]-alpha-L-lyxofuranosyl}-9H-purin-6-amine, GUANINE, ... (4 entities in total)
• 機能のキーワード: immune evasion, phosphodiesterase, poxvirus, viral protein
• 由来する生物種: Penguinpox virus
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 92761.93

構造登録者

Hobbs, S.J.,Nomburg, J.,Doudna, J.A.,Kranzusch, P.J. (登録日: 2024-04-29, 公開日: 2024-09-04, 最終更新日: 2024-10-16)

主引用文献

Hobbs, S.J.,Nomburg, J.,Doudna, J.A.,Kranzusch, P.J.
Animal and bacterial viruses share conserved mechanisms of immune evasion.
Cell, 187:5530-5539.e8, 2024

PubMed Abstract: Animal and bacterial cells sense and defend against viral infections using evolutionarily conserved antiviral signaling pathways. Here, we show that viruses overcome host signaling using mechanisms of immune evasion that are directly shared across the eukaryotic and prokaryotic kingdoms of life. Structures of animal poxvirus proteins that inhibit host cGAS-STING signaling demonstrate architectural and catalytic active-site homology shared with bacteriophage Acb1 proteins, which inactivate CBASS anti-phage defense. In bacteria, phage Acb1 proteins are viral enzymes that degrade host cyclic nucleotide immune signals. Structural comparisons of poxvirus protein-2'3'-cGAMP and phage Acb1-3'3'-cGAMP complexes reveal a universal mechanism of host nucleotide immune signal degradation and explain kingdom-specific additions that enable viral adaptation. Chimeric bacteriophages confirm that animal poxvirus proteins are sufficient to evade immune signaling in bacteria. Our findings identify a mechanism of immune evasion conserved between animal and bacterial viruses and define shared rules that explain host-virus interactions across multiple kingdoms of life.

PubMed: 39197447
DOI: 10.1016/j.cell.2024.07.057

実験手法

X-RAY DIFFRACTION (2.1 Å)