5O0I
ADP-dependent glucokinase from Pyrococcus horikoshii
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | BESSY BEAMLINE 14.1 |
Synchrotron site | BESSY |
Beamline | 14.1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-04-26 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.9184 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 77.135, 77.135, 133.889 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 44.630 - 2.000 |
R-factor | 0.1709 |
Rwork | 0.168 |
R-free | 0.21910 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1l2l |
RMSD bond length | 0.012 |
RMSD bond angle | 1.146 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX (1.10.1_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 47.300 | 2.072 |
High resolution limit [Å] | 2.000 | 2.000 |
Rmeas | 0.264 | 1.835 |
Number of reflections | 31825 | |
<I/σ(I)> | 13.44 | 1.9 |
Completeness [%] | 99.9 | 99.2 |
Redundancy | 19.78 | 20 |
CC(1/2) | 0.997 | 0.556 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 293 | 15% (w/v) PEG 6000, 0.2 M LiSO4, and 0.1 M citrate buffer (pH 3.6) |