5D9T
Crystal structure of dehydroascorbate reductase (OsDHAR) from Oryza sativa L. japonica
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 5C (4A) |
Synchrotron site | PAL/PLS |
Beamline | 5C (4A) |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-07-10 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 47.030, 48.380, 51.830 |
Unit cell angles | 90.00, 107.41, 90.00 |
Refinement procedure
Resolution | 24.728 - 1.900 |
R-factor | 0.1558 |
Rwork | 0.154 |
R-free | 0.19630 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.019 |
RMSD bond angle | 1.757 |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 2.000 |
High resolution limit [Å] | 1.900 | 1.900 |
Rmerge | 0.120 | |
Number of reflections | 17080 | |
<I/σ(I)> | 12.1 | |
Completeness [%] | 97.0 | 97.1 |
Redundancy | 6.8 | 7.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 298 | 30%(w/v) PEG MME 2000, 0.15M potassium bromide |