4NR2
Crystal structure of STK4 (MST1) SARAH domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-04-19 |
Detector | PSI PILATUS 6M |
Wavelength(s) | 0.97949 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 55.260, 63.750, 144.740 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 55.270 - 2.000 |
R-factor | 0.20866 |
Rwork | 0.207 |
R-free | 0.24033 |
Structure solution method | SIRAS |
RMSD bond length | 0.016 |
RMSD bond angle | 1.592 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SHARP |
Refinement software | REFMAC (5.8.0049) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 63.750 | 2.110 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmerge | 0.064 | 0.768 |
Number of reflections | 34702 | |
<I/σ(I)> | 11.7 | 2.2 |
Completeness [%] | 98.4 | 98 |
Redundancy | 4.4 | 4.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.5 | 277.15 | 2.3M sodium formate, 0.1M acetate pH 4.5, VAPOR DIFFUSION, SITTING DROP, temperature 277.15K |