8S0M
Crystal structure of the HKU1 receptor binding domain in complex with TMPRSS2 and the nanobody A01
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SOLEIL BEAMLINE PROXIMA 1 |
Synchrotron site | SOLEIL |
Beamline | PROXIMA 1 |
Temperature [K] | 283 |
Detector technology | PIXEL |
Collection date | 2023-09-23 |
Detector | DECTRIS EIGER X 16M |
Wavelength(s) | 0.9786 |
Spacegroup name | P 61 |
Unit cell lengths | 201.870, 201.870, 210.300 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 24.970 - 3.550 |
R-factor | 0.1943 |
Rwork | 0.193 |
R-free | 0.22130 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.004 |
RMSD bond angle | 0.788 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX ((1.20.1_4487: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.000 | 3.640 |
High resolution limit [Å] | 3.550 | 3.550 |
Rmerge | 0.265 | |
Number of reflections | 58457 | 4358 |
<I/σ(I)> | 14.6 | 0.4 |
Completeness [%] | 99.6 | 100 |
Redundancy | 43.3 | 41.4 |
CC(1/2) | 1.000 | 0.223 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 277 | 0.35 M NaH2PO4, 0.65 M K2HPO4 |