3U2L
Crystal structure of human ALR mutant C142S.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SEALED TUBE |
Source details | OXFORD DIFFRACTION ENHANCE ULTRA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-07-14 |
Detector | OXFORD ONYX CCD |
Wavelength(s) | 1.541 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 50.894, 76.641, 62.560 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 25.450 - 1.950 |
R-factor | 0.19557 |
Rwork | 0.189 |
R-free | 0.26476 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3o55 |
RMSD bond length | 0.022 |
RMSD bond angle | 1.816 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.450 | 2.000 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.100 | 0.440 |
Number of reflections | 9237 | |
<I/σ(I)> | 6.6 | 1.8 |
Completeness [%] | 99.9 | 99.9 |
Redundancy | 11.3 | 9.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6 | 298 | 0.1 M MES, 20% PEG6000, pH 6.0, VAPOR DIFFUSION, SITTING DROP, temperature 298K |