2WWU
Crystal structure of the catalytic domain of PHD finger protein 8
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-10-14 |
Detector | ADSC CCD |
Spacegroup name | I 21 3 |
Unit cell lengths | 150.980, 150.980, 150.980 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.760 - 2.150 |
R-factor | 0.1773 |
Rwork | 0.175 |
R-free | 0.21150 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2yu1 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.029 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 106.750 | 2.210 |
High resolution limit [Å] | 2.150 | 2.150 |
Rmerge | 0.080 | 0.810 |
Number of reflections | 31194 | |
<I/σ(I)> | 16.6 | 2 |
Completeness [%] | 98.0 | 99 |
Redundancy | 9.7 | 9.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 1.5 M (NH4)2SO4, 0.1 M SODIUM ACETATE PH 4.25 |