5HYD
Crystal structure of calcium-free human S100Z
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2013-09-15 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.976 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 34.326, 96.948, 115.572 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.799 - 2.300 |
R-factor | 0.2135 |
Rwork | 0.210 |
R-free | 0.26720 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2wce |
RMSD bond length | 0.004 |
RMSD bond angle | 0.642 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | PHENIX ((dev_2621: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.800 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.130 | 0.800 |
Number of reflections | 17889 | |
<I/σ(I)> | 3.3 | 1 |
Completeness [%] | 97.1 | 90.9 |
Redundancy | 5.5 | 3.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 293 | 0.1 M sodium cacodylate, 0.2 M sodium acetate, 30% PEG 8000 |