4XZM
Crystal structure of the methylated wild-type AKR1B10 holoenzyme
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06DA |
Synchrotron site | SLS |
Beamline | X06DA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-03-14 |
Detector | DECTRIS PILATUS 2M |
Wavelength(s) | 0.92020 |
Spacegroup name | P 31 |
Unit cell lengths | 79.435, 79.435, 49.796 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 34.396 - 1.750 |
R-factor | 0.2054 |
Rwork | 0.203 |
R-free | 0.24990 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1zua |
RMSD bond length | 0.008 |
RMSD bond angle | 1.266 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8_1069)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.810 |
High resolution limit [Å] | 1.750 | 1.750 |
Rmerge | 0.375 | |
Number of reflections | 35411 | |
<I/σ(I)> | 16.64 | 2.97 |
Completeness [%] | 99.0 | 100 |
Redundancy | 3.2 | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 9 | 293 | 30% PEG 6000, 100 mM sodium cacodylate |