7AXC
Crystal structure of the hPXR-LBD in complex with ferutinine
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 | 2016-06-20 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.8729 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 91.881, 91.881, 85.632 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.090 - 2.050 |
R-factor | 0.2068 |
Rwork | 0.204 |
R-free | 0.25120 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1ilg |
RMSD bond length | 0.002 |
RMSD bond angle | 0.524 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHENIX |
Refinement software | PHENIX (1.18.2_3874) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 41.090 | 2.120 |
High resolution limit [Å] | 2.050 | 2.050 |
Rmerge | 0.057 | 0.670 |
Number of reflections | 22733 | 2286 |
<I/σ(I)> | 17.9 | 2.5 |
Completeness [%] | 96.5 | 99.4 |
Redundancy | 5.7 | 5.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 291 | 50 - 100 mM imidazole 8 - 14% isopropanol |