5ELQ
Crystal structure of the SNX27 PDZ domain bound to the C-terminal DGKzeta 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) | 0.95370 |
Spacegroup name | P 2 21 21 |
Unit cell lengths | 48.940, 54.120, 74.240 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 14.900 - 1.100 |
R-factor | 0.1636 |
Rwork | 0.163 |
R-free | 0.18030 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4z8j |
RMSD bond length | 0.008 |
RMSD bond angle | 1.271 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (1.8.4_1496) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 14.900 | 1.160 |
High resolution limit [Å] | 1.100 | 1.100 |
Rmerge | 0.099 | 0.820 |
Number of reflections | 80541 | |
<I/σ(I)> | 14.5 | 3.3 |
Completeness [%] | 99.8 | 99.6 |
Redundancy | 13.2 | 12.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 293 | 2.0 M Ammonium citrate, 5% PEG400 |