Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL17U |
Synchrotron site | SSRF |
Beamline | BL17U |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2011-04-24 |
Wavelength(s) | 0.9791 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 47.540, 102.340, 47.060 |
Unit cell angles | 90.00, 92.13, 90.00 |
Refinement procedure
Resolution | 32.318 - 2.300 |
R-factor | 0.2234 |
Rwork | 0.222 |
R-free | 0.26900 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3a7s |
RMSD bond length | 0.008 |
RMSD bond angle | 1.044 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | PHASER |
Refinement software | PHENIX (1.7.1_743) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.380 |
High resolution limit [Å] | 2.300 | 2.300 |
Number of reflections | 19479 | |
Completeness [%] | 96.9 | 99 |
Redundancy | 5.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 293 | 0.2M Calcium Acetate hydrate, 0.1M Sodium Cacodylate, 18% w/v PEG 8000, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K |