5BJR
Crystal structure of the N-terminal RRM domain from MEC-8
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-2 |
Synchrotron site | ESRF |
Beamline | ID23-2 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-12-05 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 0.873 |
Spacegroup name | I 2 2 2 |
Unit cell lengths | 52.590, 96.420, 109.990 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 35.360 - 2.600 |
R-factor | 0.2421 |
Rwork | 0.237 |
R-free | 0.28530 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3md1 |
RMSD bond length | 0.002 |
RMSD bond angle | 0.571 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | BALBES |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.360 | 2.760 |
High resolution limit [Å] | 2.600 | 2.600 |
Rmerge | 0.085 | 0.344 |
Number of reflections | 8842 | |
<I/σ(I)> | 6 | |
Completeness [%] | 98.9 | |
Redundancy | 1.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293 | 0.1 M sodium acetate pH 6.5, 0.2 M ammonium sulfate, PEG 4000 30% w/v |