7XRY
Crystal structure of MERS main protease in complex with inhibitor YH-53
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL02U1 |
Synchrotron site | SSRF |
Beamline | BL02U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-03-12 |
Detector | DECTRIS EIGER X 9M |
Wavelength(s) | 0.97918 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 80.016, 93.800, 102.156 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 44.860 - 1.990 |
R-factor | 0.225103354667 |
Rwork | 0.224 |
R-free | 0.25347 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7vtc |
RMSD bond length | 0.007 |
RMSD bond angle | 0.921 |
Data reduction software | autoPROC |
Data scaling software | autoPROC |
Phasing software | PHENIX |
Refinement software | PHENIX (1.12_2829) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.860 | 2.090 |
High resolution limit [Å] | 1.990 | 1.990 |
Rmerge | 0.062 | 0.926 |
Number of reflections | 53633 | 53633 |
<I/σ(I)> | 11 | |
Completeness [%] | 99.9 | |
Redundancy | 9.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 0.2M Sodium formate, 0.1M BICINE pH8.5 20% PEG5000 |