3EAD
Crystal structure of CALX-CBD1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2005-08-11 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 1.90682 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 59.372, 73.722, 129.713 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.590 - 2.250 |
R-factor | 0.21279 |
Rwork | 0.210 |
R-free | 0.26933 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dpk |
RMSD bond length | 0.019 |
RMSD bond angle | 1.955 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.600 | 2.300 |
High resolution limit [Å] | 2.250 | 2.250 |
Rmerge | 0.072 | 0.544 |
Number of reflections | 26203 | |
<I/σ(I)> | 3.1 | |
Completeness [%] | 94.4 | 71.8 |
Redundancy | 6.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 6 | 291 | 50 mM MES, 20% PEG 3350, pH 6.0, VAPOR DIFFUSION, temperature 291K |