2BVA
Crystal structure of the human P21-activated kinase 4
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 | 2005-04-23 |
Detector | MARRESEARCH |
Spacegroup name | P 32 |
Unit cell lengths | 118.110, 118.110, 55.530 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 20.000 - 2.300 |
R-factor | 0.1878 |
R-free | 0.26860 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1u5r |
RMSD bond length | 0.007 |
RMSD bond angle | 0.023 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | SHELXL-97 |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.400 | 2.400 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.060 | 0.280 |
Number of reflections | 38417 | |
<I/σ(I)> | 11.86 | 3.55 |
Completeness [%] | 99.8 | 100 |
Redundancy | 2.7 | 2.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | SITTING DROPS, 1.5 M NACL, 10% ETHANOL |