6T1V
Structure of PPARg H494Y mutant in complex with GW1929
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID30B |
Synchrotron site | ESRF |
Beamline | ID30B |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-09-12 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.968 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 56.349, 120.741, 149.843 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 52.740 - 2.210 |
R-factor | 0.1685 |
Rwork | 0.166 |
R-free | 0.19550 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4xld |
RMSD bond length | 0.002 |
RMSD bond angle | 0.512 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 52.740 | 2.290 |
High resolution limit [Å] | 2.210 | 2.210 |
Number of reflections | 25902 | 2559 |
<I/σ(I)> | 17.9 | |
Completeness [%] | 99.8 | |
Redundancy | 2 | |
CC(1/2) | 0.999 | 0.842 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 290 | 0.2 M ammonium acetate, 0.1 M Hepes pH 7.5, trisodium citrate 1.2M |