8CH8
Crystal structure of the human PXR ligand-binding domain in complex with liranaftate
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2022-10-07 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.619923 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 91.649, 91.649, 85.744 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 64.810 - 2.150 |
R-factor | 0.2072 |
Rwork | 0.206 |
R-free | 0.22810 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.003 |
RMSD bond angle | 0.708 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | MOLREP |
Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 64.810 | 2.230 |
High resolution limit [Å] | 2.150 | 2.150 |
Rmerge | 0.043 | 0.751 |
Number of reflections | 20353 | 1519 |
<I/σ(I)> | 19.3 | |
Completeness [%] | 90.1 | |
Redundancy | 6.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 291 | 50-100 mM IMIDAZOLE, 8-14% ISOPROPANOL |