7NEO
Crystal Structure of SARS-CoV-2 main protease (Nsp5) in complex with compound 15
This is a non-PDB format compatible entry.
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | MAX IV BEAMLINE BioMAX |
| Synchrotron site | MAX IV |
| Beamline | BioMAX |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2020-12-20 |
| Detector | DECTRIS EIGER X 16M |
| Wavelength(s) | 0.976 |
| Spacegroup name | P 1 21 1 |
| Unit cell lengths | 44.572, 53.822, 114.768 |
| Unit cell angles | 90.00, 100.49, 90.00 |
Refinement procedure
| Resolution | 48.627 - 1.640 |
| Rwork | 0.201 |
| R-free | 0.23870 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7b2j |
| RMSD bond length | 0.011 |
| RMSD bond angle | 1.704 |
| Data reduction software | XDS (b. 20200131) |
| Data scaling software | Aimless (0.7.4) |
| Phasing software | PHASER (2.8.2) |
| Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 48.670 | 1.670 |
| High resolution limit [Å] | 1.640 | 1.640 |
| Rmerge | 0.065 | 0.431 |
| Rmeas | 0.079 | 0.529 |
| Rpim | 0.045 | 0.302 |
| Number of reflections | 65712 | 3232 |
| <I/σ(I)> | 11.3 | 3.2 |
| Completeness [%] | 99.9 | 100 |
| Redundancy | 5.6 | 5.6 |
| CC(1/2) | 0.998 | 0.940 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.75 | 293 | 100 nL protein (8.3 mg/mL, 50 mM Tris pH 8.0, 300 mM NaCl), 50 nL seeds, 450 nL reservoir (200 mM HEPES pH 7.75, 5% DMSO, 12.5% PEG4K). Soaking: 200 mM HEPES pH 7.75, 12 mM compound, 5% DMSO, 10% PEG300, 20% PEG3K, RT, 2 h. |






