2XWC
Crystal structure of the DNA binding domain of human TP73 refined at 1.8 A resolution
Replaces: 2XIPExperimental 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 | 2010-05-26 |
Detector | ADSC CCD |
Spacegroup name | P 43 3 2 |
Unit cell lengths | 110.370, 110.370, 110.370 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.360 - 1.820 |
R-factor | 0.1909 |
Rwork | 0.189 |
R-free | 0.22824 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 20CJ |
RMSD bond length | 0.016 |
RMSD bond angle | 1.542 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.5.0110) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.360 | 49.360 |
High resolution limit [Å] | 1.820 | 1.820 |
Rmerge | 0.160 | 1.240 |
Number of reflections | 280763 | |
<I/σ(I)> | 11.9 | 2 |
Completeness [%] | 100.0 | 100 |
Redundancy | 13.2 | 12.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 1.2M SODIUM POTASSIUM TARTRATE, 0.25% PEG MME 5000, 0.1M TRIS PH 9 |