7AXK
Crystal structure of the hPXR-LBD in complex with estradiol and endosulfan
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-2 |
Synchrotron site | ESRF |
Beamline | ID23-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2015-07-17 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 0.87260 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 92.109, 92.109, 86.120 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 46.050 - 2.000 |
R-factor | 0.1804 |
Rwork | 0.179 |
R-free | 0.21180 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1ilg |
RMSD bond length | 0.009 |
RMSD bond angle | 1.114 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | PHENIX |
Refinement software | PHENIX (1.18_3845) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 46.060 | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmeas | 0.080 | 0.442 |
Number of reflections | 25602 | 3643 |
<I/σ(I)> | 13.6 | 3.8 |
Completeness [%] | 99.9 | 100 |
Redundancy | 6.9 | 7.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 291 | 50 - 100 mM imidazole 8 - 14% isopropanol |