5UHK
Crystal structure of the core catalytic domain of Human O-GlcNAcase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 17-ID |
Synchrotron site | APS |
Beamline | 17-ID |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2012-03-30 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 1.00 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 96.800, 96.800, 256.960 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 34.240 - 2.970 |
R-factor | 0.197 |
Rwork | 0.194 |
R-free | 0.25100 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.120 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | BUSTER (2.11.6) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 128.000 | 2.980 |
High resolution limit [Å] | 2.970 | 2.970 |
Rmerge | 0.077 | 1.055 |
Number of reflections | 24942 | |
<I/σ(I)> | 22.3 | 2.2 |
Completeness [%] | 95.9 | 100 |
Redundancy | 12.8 | 12.6 |
CC(1/2) | 0.999 | 0.927 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293 | 14-17% PEG 3350, 0.2 M Mg Formate |