9FX6
Crystal structure of Cryo2RT SARS-CoV-2 main protease at 100K
Summary for 9FX6
Entry DOI | 10.2210/pdb9fx6/pdb |
Descriptor | 3C-like proteinase nsp5, DIMETHYL SULFOXIDE, SULFATE ION, ... (5 entities in total) |
Functional Keywords | cryo2rt, synchrotron, room-temperature, protein, viral protein |
Biological source | Severe acute respiratory syndrome coronavirus 2 |
Total number of polymer chains | 2 |
Total formula weight | 68258.19 |
Authors | Huang, C.Y.,Aumonier, S.,Mac Sweeney, A.,Olieric, V.,Wang, M. (deposition date: 2024-07-01, release date: 2024-07-31, Last modification date: 2024-08-14) |
Primary citation | 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 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.227 Å) |
Structure validation
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