7H5O
Crystal structure of endothiapepsin PF_cryo3 in complex with TL00150 at 100 K
7H5O の概要
エントリーDOI | 10.2210/pdb7h5o/pdb |
Group deposition | A High-Throughput Method for Room-Temperature Macromolecular Crystallography from Frozen Crystals (G_1002290) |
分子名称 | Endothiapepsin, ACETATE ION, DIMETHYL SULFOXIDE, ... (4 entities in total) |
機能のキーワード | endopeptidase, hydrolase, room temperature |
由来する生物種 | Cryphonectria parasitica (chestnut blight fungus) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 36529.42 |
構造登録者 | Huang, C.-Y.,Aumonier, S.,Olieric, V.,Wang, M. (登録日: 2024-04-10, 公開日: 2024-08-07, 最終更新日: 2024-10-23) |
主引用文献 | Huang, C.Y.,Aumonier, S.,Olieric, V.,Wang, M. Cryo2RT: a high-throughput method for room-temperature macromolecular crystallography from cryo-cooled crystals. Acta Crystallogr D Struct Biol, 80:620-628, 2024 Cited by PubMed Abstract: Advances in structural biology have relied heavily on synchrotron cryo-crystallography and cryogenic electron microscopy to elucidate biological processes and for drug discovery. However, disparities between cryogenic and room-temperature (RT) crystal structures pose challenges. Here, Cryo2RT, a high-throughput RT data-collection method from cryo-cooled crystals that leverages the cryo-crystallography workflow, is introduced. Tested on endothiapepsin crystals with four soaked fragments, thaumatin and SARS-CoV-2 3CL, Cryo2RT reveals unique ligand-binding poses, offers a comparable throughput to cryo-crystallography and eases the exploration of structural dynamics at various temperatures. PubMed: 39052318DOI: 10.1107/S2059798324006697 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.39 Å) |
構造検証レポート
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