6VZL
Crystal structure of human PPARgamma ligand binding domain in complex with GW1929
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 | 2018-08-18 |
| Detector | DECTRIS PILATUS3 6M |
| Wavelength(s) | 0.97946 |
| Spacegroup name | C 1 2 1 |
| Unit cell lengths | 92.849, 62.131, 119.116 |
| Unit cell angles | 90.00, 102.17, 90.00 |
Refinement procedure
| Resolution | 58.220 - 2.070 |
| R-factor | 0.253 |
| Rwork | 0.251 |
| R-free | 0.28860 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 1prg |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.004 |
| Data reduction software | MOSFLM |
| Data scaling software | SCALA |
| Phasing software | PHASER |
| Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 58.220 | 2.144 |
| High resolution limit [Å] | 2.070 | 2.070 |
| Rmerge | 0.051 | 1.374 |
| Rmeas | 0.056 | |
| Rpim | 0.022 | |
| Number of reflections | 40606 | 3920 |
| <I/σ(I)> | 13.59 | |
| Completeness [%] | 98.8 | 97.88 |
| Redundancy | 6.4 | 6.4 |
| CC(1/2) | 0.999 | 0.727 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.4 | 293 | 0.1M MOPS, pH 7.4, 0.8M SODIUM CITRATE |






