5EMB
Crystal structure of the SNX27 PDZ domain bound to the C-terminal phosphorylated PTHR PDZ binding motif
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2015-10-01 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.70850 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 37.570, 48.330, 56.177 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 10.200 - 0.850 |
R-factor | 0.12397 |
Rwork | 0.124 |
R-free | 0.13567 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4z8j |
RMSD bond length | 0.022 |
RMSD bond angle | 2.089 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 31.265 | 0.860 |
High resolution limit [Å] | 0.850 | 0.850 |
Rmerge | 2.060 | |
Number of reflections | 90806 | |
<I/σ(I)> | 25.9 | 2.8 |
Completeness [%] | 98.7 | 100 |
Redundancy | 14 | 13.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 293 | 10% PEG1000, 10% PEG8000 |