7SF1
SARS-CoV-2 Main Protease (Mpro) in Complex with ML1001
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL12-1 |
Synchrotron site | SSRL |
Beamline | BL12-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2020-12-05 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.97946 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 114.548, 52.925, 45.190 |
Unit cell angles | 90.00, 103.32, 90.00 |
Refinement procedure
Resolution | 39.220 - 1.850 |
R-factor | 0.1652 |
Rwork | 0.163 |
R-free | 0.20790 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 6lze |
RMSD bond length | 0.009 |
RMSD bond angle | 1.543 |
Data reduction software | XDS |
Data scaling software | SCALA (3.3.22) |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0267) |
Data quality characteristics
Overall | Inner shell | Outer shell | |
Low resolution limit [Å] | 55.733 | 39.192 | 1.950 |
High resolution limit [Å] | 1.850 | 5.850 | 1.850 |
Rmerge | 0.055 | 0.611 | |
Rmeas | 0.096 | 0.063 | 0.708 |
Rpim | 0.048 | 0.031 | 0.353 |
Total number of observations | 86585 | 2889 | 12688 |
Number of reflections | 22318 | 746 | 3233 |
<I/σ(I)> | 6.9 | 16.2 | 1.8 |
Completeness [%] | 98.8 | 99.1 | 99.2 |
Redundancy | 3.9 | 3.9 | 3.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 289.15 | Sitting drops consisted of 0.16 uL A:0.16 uL B: A) 5 mg/mL Mpro + 1.5 mM ML1001 in in 20 mM Tris pH 7.3 + 2 mM DTT + 5 % DMSO B) 0.1 M HEPES pH 7.5 + 0.2 M L-Proline + 24 % w/v PEG 1500 |