2JAM
Crystal structure of human calmodulin-dependent protein kinase I G
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 | 2006-10-19 |
Detector | MARRESEARCH |
Spacegroup name | P 1 |
Unit cell lengths | 51.666, 53.736, 64.177 |
Unit cell angles | 65.45, 71.91, 73.84 |
Refinement procedure
Resolution | 56.890 - 1.700 |
R-factor | 0.157 |
Rwork | 0.155 |
R-free | 0.23100 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1a06 |
RMSD bond length | 0.013 |
RMSD bond angle | 1.364 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 33.360 | 1.790 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.050 | 0.280 |
Number of reflections | 64017 | |
<I/σ(I)> | 12.82 | 2.97 |
Completeness [%] | 98.9 | 93 |
Redundancy | 2.79 | 2.31 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 0.20M NA(MALONATE), 0.1M BTPROP PH 7.5, 20.0% PEG 3350, 10.0% ETGLY |