6TKY
Crystal structure of the DHR2 domain of DOCK10 in complex with CDC42
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2010-09-09 |
Detector | DECTRIS PILATUS3 2M |
Wavelength(s) | 0.979 |
Spacegroup name | P 41 21 2 |
Unit cell lengths | 96.898, 96.898, 310.910 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.830 - 2.550 |
R-factor | 0.1913 |
Rwork | 0.188 |
R-free | 0.24640 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2wm9 |
RMSD bond length | 0.008 |
RMSD bond angle | 0.929 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.17.1_3660) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 29.830 | 2.640 |
High resolution limit [Å] | 2.550 | 2.550 |
Number of reflections | 49296 | 5918 |
<I/σ(I)> | 5.52 | |
Completeness [%] | 99.9 | |
Redundancy | 7.23 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 7.5 | 293 | 25% (w/v) PEG 3350, 200 mM potassium acetate, 8% (v/v) 1,1,1,3,3,3-Hexafluoro-2-propanol. |