2HW7
Crystal Structure of Mnk2-D228G in complex with Staurosporine
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2005-08-10 |
Detector | MAR scanner 345 mm plate |
Wavelength(s) | 0.98008 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 102.366, 102.366, 76.439 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 30.000 - 2.710 |
R-factor | 0.2034 |
Rwork | 0.201 |
R-free | 0.24566 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2ac3 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.389 |
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] | 2.700 |
Number of reflections | 12862 |
Completeness [%] | 99.7 |
Redundancy | 5.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7.6 | 293 | Polyacrylic acid, pH 7.6, VAPOR DIFFUSION, temperature 293K |