4PQP
Crystal structure of human SNX14 PX domain in space group P43212
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 121.670, 121.670, 82.430 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.948 - 3.000 |
R-factor | 0.2368 |
Rwork | 0.234 |
R-free | 0.28560 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.011 |
RMSD bond angle | 1.452 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.8.1_1168)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 68.200 | |
High resolution limit [Å] | 3.000 | 3.000 |
Rmerge | 0.140 | |
Number of reflections | 12933 | |
Completeness [%] | 100.0 | |
Redundancy | 27.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.5 | 293 | 20% PEG4000, 0.1 M sodium citrate tribasic, pH 4.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K |