2VV0
hPPARgamma Ligand binding domain in complex with DHA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-3 |
Synchrotron site | ESRF |
Beamline | ID14-3 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-11-16 |
Detector | ADSC CCD |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 93.090, 61.280, 118.550 |
Unit cell angles | 90.00, 103.19, 90.00 |
Refinement procedure
Resolution | 35.910 - 2.550 |
R-factor | 0.218 |
Rwork | 0.218 |
R-free | 0.26100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2i4p |
RMSD bond length | 0.010 |
RMSD bond angle | 1.200 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | CNS (1.2) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 57.740 | 2.690 |
High resolution limit [Å] | 2.550 | 2.550 |
Rmerge | 0.060 | 0.300 |
Number of reflections | 40468 | |
<I/σ(I)> | 16.6 | 3.9 |
Completeness [%] | 99.0 | 97.4 |
Redundancy | 3.5 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 8 | 295 | PH 8, TRIS 100MM, 0.7M NACITRATE, 1MM TCEP, 0.5MM EDTA, VAPOUR DIFFUSION, DARK, UNDER NITROGEN, 22 DEGREES CELSIUS |