2REA
Crystal structures of C2ALPHA-PI3 kinase PX-domain domain indicate conformational change associated with ligand binding.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 105 |
Detector technology | IMAGE PLATE |
Collection date | 2004-11-04 |
Detector | RIGAKU RAXIS IV |
Wavelength(s) | 1.5418 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 56.866, 56.866, 92.995 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 27.190 - 2.500 |
R-factor | 0.23454 |
Rwork | 0.231 |
R-free | 0.31808 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1ocs |
RMSD bond length | 0.034 |
RMSD bond angle | 2.814 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | EPMR |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.028 | 0.107 |
Number of reflections | 5731 | |
<I/σ(I)> | 40 | 9 |
Completeness [%] | 89.4 | 70.9 |
Redundancy | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 293 | 0.1M MALEIC ACID/NAOH, 10% GLYCEROL, PH 6.00, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 293K |