2HW6
Crystal structure of Mnk1 catalytic domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-04-04 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 0.98008 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 93.468, 93.468, 175.181 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.000 - 2.500 |
R-factor | 0.20911 |
Rwork | 0.207 |
R-free | 0.25701 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2ac3 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.174 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 30.000 |
High resolution limit [Å] | 2.500 |
Number of reflections | 18256 |
Completeness [%] | 92.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 5.6 | 293 | 20% PEG3350, 0.2M Ammonium sulfate, pH 5.6, VAPOR DIFFUSION, temperature 293K |