5CA5
Structure of the C. elegans NONO-1 homodimer
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 | PIXEL |
Collection date | 2013-11-13 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.96580 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 60.318, 63.115, 83.838 |
Unit cell angles | 90.00, 101.03, 90.00 |
Refinement procedure
Resolution | 19.670 - 2.400 |
R-factor | 0.246 |
Rwork | 0.243 |
R-free | 0.30080 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4wii |
RMSD bond length | 0.010 |
RMSD bond angle | 1.160 |
Data reduction software | XDS |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | BUSTER (2.10.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.670 | 2.530 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.800 | |
Number of reflections | 23755 | |
<I/σ(I)> | 1.4 | |
Completeness [%] | 92.4 | |
Redundancy | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 293.15 | 0.1 M HEPES, 0.1 M Ammonium sulphate, 15.0 - 20.0 % PEG 3350 |