2F57
Crystal Structure Of The Human P21-Activated Kinase 5
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 | 2005-10-22 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.9788 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 98.661, 56.599, 120.764 |
Unit cell angles | 90.00, 103.13, 90.00 |
Refinement procedure
Resolution | 50.000 - 1.800 |
R-factor | 0.15525 |
Rwork | 0.154 |
R-free | 0.18513 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ID 2C30 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.226 |
Data reduction software | HKL-2000 |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.860 |
High resolution limit [Å] | 1.800 | 1.800 |
Number of reflections | 60040 | |
Completeness [%] | 99.4 | 94 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 8 | 277 | 0.2M Na/KPO4, 0.1M BTProp 7.5, 20% PEG3350, 10% Ethelene glycol, pH 8.0, VAPOR DIFFUSION, SITTING DROP, temperature 277K |