3KN5
Crystal structure of the C-terminal kinase domain of msk1 in complex with AMP-PNP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-C |
Synchrotron site | APS |
Beamline | 24-ID-C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-03-07 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 1.0000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 51.561, 91.250, 135.460 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 43.240 - 2.400 |
R-factor | 0.211 |
Rwork | 0.208 |
R-free | 0.27800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2qr8 |
RMSD bond length | 0.006 |
RMSD bond angle | 1.104 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 43.240 | 2.700 |
High resolution limit [Å] | 2.396 | 2.400 |
Rmerge | 0.118 | 0.492 |
Number of reflections | 23504 | |
<I/σ(I)> | 16 | 2.8 |
Completeness [%] | 91.0 | 85 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 7.5 | PH 7.5, VAPOR DIFFUSION |