1B34
CRYSTAL STRUCTURE OF THE D1D2 SUB-COMPLEX FROM THE HUMAN SNRNP CORE DOMAIN
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ELETTRA BEAMLINE 5.2R |
Synchrotron site | ELETTRA |
Beamline | 5.2R |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Detector | MARRESEARCH |
Spacegroup name | P 62 |
Unit cell lengths | 75.300, 75.300, 91.990 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 18.400 - 2.500 |
Rwork | 0.249 |
R-free | 0.28600 |
Structure solution method | MIR |
RMSD bond length | 0.009 |
RMSD bond angle | 0.023 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Refinement software | REFMAC |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 18.400 |
High resolution limit [Å] | 2.500 |
Rmerge | 0.049 |
Number of reflections | 10307 |
Completeness [%] | 97.4 |
Redundancy | 4.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, sitting drop * | 5.6 | pH 5.6 |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | reservoir | sodium citrate | 0.1 (M) | |
2 | 1 | reservoir | ammonium acetate | 0.2 (M) | |
3 | 1 | reservoir | glycerol | 15 (%) | |
4 | 1 | reservoir | PEG4000 | 25 (%) |