7BAE
Crystal structure of PAFB
7BAE の概要
| エントリーDOI | 10.2210/pdb7bae/pdb |
| 関連するPDBエントリー | 2NC2 |
| 分子名称 | Antifungal protein (2 entities in total) |
| 機能のキーワード | penicillium chrysogenum antifungal protein b, calix[n]arene, porous framework, zinc, antifungal protein |
| 由来する生物種 | Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 6516.39 |
| 構造登録者 | Guagnini, F.,Huber, A.,Alex, J.M.,Marx, F.,Crowley, P.B. (登録日: 2020-12-15, 公開日: 2021-03-17, 最終更新日: 2024-11-20) |
| 主引用文献 | Guagnini, F.,Huber, A.,Alex, J.M.,Marx, F.,Crowley, P.B. Porous assembly of an antifungal protein mediated by zinc and sulfonato-calix[8]arene. J.Struct.Biol., 213:107711-107711, 2021 Cited by PubMed Abstract: Controlled protein assembly holds great potential in the fabrication of biohybrid materials. However, the structural diversity and complexity of proteins present an obstacle to controlled assembly. Supramolecular chemistry is a possible solution as it offers tools to mediate self-assembly with molecular precision. This paper deals with the calixarene- and zinc-mediated assembly and crystallization of the histidine-rich Penicillium chrysogenum antifungal protein B (PAFB). We report crystal structures of pure PAFB, PAFB in complex with Zn, and the ternary complex of PAFB, Zn and sulfonato-calix[8]arene (sclx). A comparison of the three crystal structures revealed the structural plasticity of PAFB. While the flexible and highly anionic sclx resulted in large molecular weight aggregates of PAFB in solution, diffraction-quality crystals of PAFB-sclx were not obtained. We report crystals of PAFB-Zn-sclx in which a trinuclear zinc cluster occurred adjacent to a calixarene binding site. Interestingly, the combination of sclx complexation and zinc coordination resulted in a porous framework with channels of circa 2 nm diameter. Detailed analysis of the crystal structure highlighted novel molecular recognition features. This research enriches the set of supramolecular interactions available to promote protein assembly. PubMed: 33631304DOI: 10.1016/j.jsb.2021.107711 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.2 Å) |
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