6KOR
Crystal structure of the RRM domain of SYNCRIP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU MICROMAX-007 HF |
Temperature [K] | 193.15 |
Detector technology | CCD |
Collection date | 2018-04-06 |
Detector | RIGAKU |
Wavelength(s) | 1.54187 |
Spacegroup name | H 3 |
Unit cell lengths | 103.634, 103.634, 49.289 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 25.908 - 2.602 |
R-factor | 0.1855 |
Rwork | 0.182 |
R-free | 0.24990 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dgu |
RMSD bond length | 0.010 |
RMSD bond angle | 1.146 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | CRANK2 |
Refinement software | PHENIX (1.14_3260) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 25.908 | 2.640 |
High resolution limit [Å] | 2.602 | 2.602 |
Rmerge | 0.049 | |
Number of reflections | 6026 | 6026 |
<I/σ(I)> | 11.2 | |
Completeness [%] | 99.7 | |
Redundancy | 4.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 293.15 | 0.1M HEPES-NaOH (pH 7.5), 20% PEG 10,000 |