4DNN
Crystal structure of the Quaking Qua1 homodimerization domain
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | SSRL BEAMLINE BL11-1 |
Synchrotron site | SSRL |
Beamline | BL11-1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-02-01 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.9791358, 0.9184018, 0.979569 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 33.983, 36.024, 92.814 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 31.911 - 2.100 |
R-factor | 0.2179 |
Rwork | 0.216 |
R-free | 0.25150 |
Structure solution method | MAD |
RMSD bond length | 0.008 |
RMSD bond angle | 1.102 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX ((phenix.refine: 1.7.2_869)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.650 |
High resolution limit [Å] | 2.100 | 2.100 |
Number of reflections | 7046 | |
<I/σ(I)> | 35.1 | 5.2 |
Redundancy | 4.3 | 4.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 295 | sodium cacodylate, calcium acetate, PEG 600, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 295K |