8ZFO
Crystal Structure of Human PPARgamma Ligand Binding Domain in Complex with GW9662 and nTZDpa
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.2 |
Synchrotron site | ALS |
Beamline | 5.0.2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2017-08-16 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.97741 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 92.750, 62.216, 119.077 |
Unit cell angles | 90.00, 102.19, 90.00 |
Refinement procedure
Resolution | 49.159 - 3.150 |
R-factor | 0.22 |
Rwork | 0.212 |
R-free | 0.29610 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.013 |
RMSD bond angle | 1.464 |
Data reduction software | DIALS |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.160 | 3.263 |
High resolution limit [Å] | 3.150 | 3.150 |
Number of reflections | 11672 | 1161 |
<I/σ(I)> | 15.02 | |
Completeness [%] | 99.6 | 100 |
Redundancy | 2 | 2 |
CC(1/2) | 0.998 | 0.916 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.6 | 293 | 0.8M SODIUM CITRATE, 100mM MOPS, pH 7.6 |