2JC6
Crystal structure of human calmodulin-dependent protein kinase 1D
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 | 2006-11-27 |
Detector | MARRESEARCH |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 39.640, 93.060, 101.860 |
Unit cell angles | 90.00, 96.16, 90.00 |
Refinement procedure
Resolution | 101.020 - 2.300 |
R-factor | 0.189 |
Rwork | 0.186 |
R-free | 0.24800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1a06 |
RMSD bond length | 0.013 |
RMSD bond angle | 1.428 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.200 | 2.400 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.100 | 0.440 |
Number of reflections | 29986 | |
<I/σ(I)> | 11.17 | 2.56 |
Completeness [%] | 91.6 | 99.9 |
Redundancy | 3.47 | 3.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 0.1M CITRATE PH 5.6, 20% ISOPROPANOL, 20% PEG 4K. |