3AX7
Bovine Xanthine Oxidase, protease cleaved form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PHOTON FACTORY BEAMLINE AR-NW12A |
Synchrotron site | Photon Factory |
Beamline | AR-NW12A |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-11-28 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 1 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 133.477, 73.151, 146.267 |
Unit cell angles | 90.00, 98.18, 90.00 |
Refinement procedure
Resolution | 36.370 - 2.340 |
R-factor | 0.19658 |
Rwork | 0.194 |
R-free | 0.24020 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.013 |
RMSD bond angle | 1.605 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | AMoRE |
Refinement software | REFMAC (5.5.0110) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 36.370 |
High resolution limit [Å] | 2.340 |
Number of reflections | 104898 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7.4 | 293 | 6-9% PEG 4000, 50mM potassium phosphate, 1mM salicylate, 0.2mM EDTA, 5mM DTT, 30% glycerol, pH 7.4, VAPOR DIFFUSION, temperature 293K |