4AAC
P38ALPHA MAP KINASE BOUND TO CMPD 29
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2004-11-24 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 64.511, 75.073, 76.899 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 53.680 - 2.500 |
R-factor | 0.23413 |
Rwork | 0.230 |
R-free | 0.30525 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | NONE |
RMSD bond length | 0.011 |
RMSD bond angle | 1.459 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | REFMAC (5.6.0113) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 53.680 | 2.640 |
High resolution limit [Å] | 2.500 | 2.500 |
Rmerge | 0.200 | 0.410 |
Number of reflections | 13427 | |
<I/σ(I)> | 7.4 | 3 |
Completeness [%] | 99.8 | 100 |
Redundancy | 4.7 | 4.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 298 | 6-10% PEG-MME 5000, PH 6.5, VAPOR DIFFUSION, HANGING DROP, TEMPERATURE 298K |