6KO1
The crystal structue of PDE10A complexed with 2d
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SEALED TUBE |
Source details | OXFORD DIFFRACTION NOVA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2018-01-24 |
Detector | OXFORD ONYX CCD |
Wavelength(s) | 1.5418 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 49.763, 81.401, 161.233 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.823 - 2.700 |
R-factor | 0.2382 |
Rwork | 0.233 |
R-free | 0.33950 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2oup |
RMSD bond length | 0.010 |
RMSD bond angle | 1.130 |
Data reduction software | CrysalisPro (38.42) |
Data scaling software | CrysalisPro (38.42) |
Phasing software | PHASER (1.10) |
Refinement software | PHENIX (1.10_2155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 24.823 | 2.800 |
High resolution limit [Å] | 2.700 | 2.700 |
Rmerge | 0.145 | 0.380 |
Number of reflections | 18454 | 1792 |
<I/σ(I)> | 6.4 | 2.1 |
Completeness [%] | 98.8 | 96.76 |
Redundancy | 3.4 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7.5 | 277 | 0.1 M Hepes (pH 7.5), 0.2 M MgCl2, 18% PEG 3350, 50 mM 2-mercaptoethanol |