2IHB
Crystal structure of the heterodimeric complex of human RGS10 and activated Gi alpha 3
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X10SA |
Synchrotron site | SLS |
Beamline | X10SA |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-05-06 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.97925 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 100.628, 100.628, 145.359 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 47.600 - 2.710 |
R-factor | 0.20913 |
Rwork | 0.208 |
R-free | 0.23632 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Swissmodel based on the coordinates of PDB entries 1agr 1ezt 1ezy 2bv1 |
RMSD bond length | 0.009 |
RMSD bond angle | 1.057 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.750 |
High resolution limit [Å] | 2.700 | 2.700 |
Number of reflections | 20470 | |
Completeness [%] | 97.2 | 80.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5.5 | 293 | 0.2M (NH4)2SO4, 0.1M Bis-Tris, pH 5.5, 25% PEG3350 , VAPOR DIFFUSION, SITTING DROP, temperature 293K |