4GVB

Crystal structure of the virally encoded antifungal protein, KP6, heterodimer

4GVB の概要

• エントリーDOI: 10.2210/pdb4gvb/pdb
• 分子名称: KP6 killer toxin subunit alpha, KP6 killer toxin subunit beta (3 entities in total)
• 機能のキーワード: antifungal protein, secreted, toxin
• 由来する生物種: Ustilago maydis virus P6 (UmV6); 詳細
• 細胞内の位置: Secreted: P16948 P16948
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 18036.03

構造登録者

Smith, T. (登録日: 2012-08-30, 公開日: 2012-12-19, 最終更新日: 2024-11-20)

主引用文献

Allen, A.,Chatt, E.,Smith, T.J.
The Atomic Structure of the Virally Encoded Antifungal Protein, KP6.
J.Mol.Biol., 425:609-621, 2013

PubMed Abstract: Killer toxins are produced by several genera of yeast and filamentous fungi. A small proportion of Ustilago maydis strains produce killer toxins, to which they are resistant, but sensitive strains are the majority in the wild populations. There are three killer types (P1, P4 and P6) that secrete KP1, KP4 and KP6 toxins, respectively, which are produced only by strains persistently infected with double-stranded RNA viruses (UmV) in the cell cytoplasm. Unlike nearly all other viruses, UmV are only transmitted through mitosis or meiosis. As shown here, KP6 is different from any other known cytotoxic protein. KP6 is neutral protein composed of two subunits: KP6α and KP6β. KP6α is responsible for targeting while KP6β is cytotoxic. Neither subunit is homologous in either sequence or structure to any other toxin, but they have highly similar structures to each other. The major difference between the two subunits is a hydrophobic helix at the N-terminus of KP6α and is likely key to target recognition. Unlike any other toxin, KP6 is translated as a single polypeptide with a 31-residue linker region in the middle of the protein. From structural prediction studies, this linker likely makes for a more compact KP6 structure that sequesters the hydrophobic helix of KP6α. A model whereby the protoxin undergoes a conformational activation process that exposes this helix immediately prior to secretion is presented.

PubMed: 23219466
DOI: 10.1016/j.jmb.2012.11.033

実験手法

X-RAY DIFFRACTION (1.8 Å)