6AUG
Crystal Structure of Human PPARgamma Ligand Binding Domain in Complex with SR16832
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-007 HF |
Temperature [K] | 200 |
Detector technology | IMAGE PLATE |
Collection date | 2016-10-16 |
Detector | MAR scanner 345 mm plate |
Wavelength(s) | 1.5418 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 92.610, 62.080, 118.450 |
Unit cell angles | 90.00, 102.34, 90.00 |
Refinement procedure
Resolution | 45.561 - 2.730 |
R-factor | 0.2067 |
Rwork | 0.198 |
R-free | 0.28090 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1prg |
RMSD bond length | 0.009 |
RMSD bond angle | 1.147 |
Data reduction software | iMOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 45.561 |
High resolution limit [Å] | 2.730 |
Number of reflections | 15056 |
<I/σ(I)> | 10.43 |
Completeness [%] | 85.1 |
Redundancy | 1.8 |
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 |