4L0N
Crystal structure of STK3 (MST2) 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 41 21 2 |
Unit cell lengths | 61.320, 61.320, 301.860 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.660 - 1.400 |
R-factor | 0.16279 |
Rwork | 0.160 |
R-free | 0.20667 |
Structure solution method | SAD |
RMSD bond length | 0.017 |
RMSD bond angle | 1.718 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | SHARP |
Refinement software | REFMAC (5.7.0032) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 32.840 | 1.480 |
High resolution limit [Å] | 1.400 | 1.400 |
Rmerge | 0.067 | 0.544 |
Number of reflections | 114371 | |
<I/σ(I)> | 12.9 | 2.9 |
Completeness [%] | 99.7 | 99.8 |
Redundancy | 5.4 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 4.9 | 277.15 | 30% MPD, 0.1M acetate pH 4.9, 0.2M calcium chloride, VAPOR DIFFUSION, SITTING DROP, temperature 277.15K |