6C80
Crystal structure of a flax cytokinin oxidase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 80 |
Detector technology | CCD |
Collection date | 2012-05-01 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.953691 |
Spacegroup name | I 1 2 1 |
Unit cell lengths | 91.226, 58.929, 188.867 |
Unit cell angles | 90.00, 95.62, 90.00 |
Refinement procedure
Resolution | 49.355 - 1.780 |
R-factor | 0.1523 |
Rwork | 0.151 |
R-free | 0.18370 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2exr |
RMSD bond length | 0.007 |
RMSD bond angle | 1.154 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 85.080 | 1.880 |
High resolution limit [Å] | 1.780 | 1.780 |
Number of reflections | 95714 | |
<I/σ(I)> | 2.8 | |
Completeness [%] | 99.8 | |
Redundancy | 7.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 293 | 0.24 M tribasic ammonium citrate (pH 8.0) and 18% (w/v) PEG-3350 |