4BC3
Crystal structure of human D-xylulokinase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | LNLS BEAMLINE W01B-MX2 |
Synchrotron site | LNLS |
Beamline | W01B-MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-08-13 |
Detector | MARRESEARCH |
Spacegroup name | P 32 |
Unit cell lengths | 99.790, 99.790, 157.540 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 58.220 - 1.680 |
R-factor | 0.1598 |
Rwork | 0.159 |
R-free | 0.18360 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | HUMAN D-XYLULOSE DETERMINED BY TWO-ENERGY SELENIUM MAD |
RMSD bond length | 0.010 |
RMSD bond angle | 1.040 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | BUSTER (2.11.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 58.250 | 1.710 |
High resolution limit [Å] | 1.680 | 1.680 |
Rmerge | 0.170 | |
Number of reflections | 200085 | |
<I/σ(I)> | 9.4 | 0.6 |
Completeness [%] | 100.0 | 100 |
Redundancy | 8.5 | 8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 200 MM MES/KOH, PH 5.9, 13% PEG 6000 |