8H82
Crystal structure of SARS-CoV-2 main protease (Mpro) Mutant (E166V) in complex with protease inhibitor Nirmatrelvir
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I04 |
Synchrotron site | Diamond |
Beamline | I04 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-08-10 |
Detector | DECTRIS EIGER2 X 16M |
Wavelength(s) | 0.953740 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 45.951, 64.037, 105.284 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 27.890 - 1.930 |
R-factor | 0.1738 |
Rwork | 0.170 |
R-free | 0.21560 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7vh8 |
Data reduction software | autoPROC |
Data scaling software | XSCALE |
Phasing software | PHENIX |
Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 27.890 | 27.890 | 2.050 |
High resolution limit [Å] | 1.930 | 5.690 | 1.930 |
Rmerge | 0.106 | 0.042 | 0.654 |
Rmeas | 0.111 | 0.044 | 0.682 |
Total number of observations | 320663 | ||
Number of reflections | 24025 | 1052 | 3773 |
<I/σ(I)> | 17.65 | 51.14 | 3.48 |
Completeness [%] | 99.8 | 98.6 | 99.3 |
Redundancy | 13.347 | 12.453 | 12.579 |
CC(1/2) | 0.999 | 0.999 | 0.904 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 293 | 0.1 M Tris pH 7.6, 14% v/v ethylene glycol, 7% w/v PEG 8,000 |