2YT4
Crystal structure of human DGCR8 core
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 4A |
Synchrotron site | PAL/PLS |
Beamline | 4A |
Temperature [K] | 113 |
Detector technology | CCD |
Collection date | 2005-10-02 |
Wavelength(s) | 0.98010 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 57.511, 59.985, 70.921 |
Unit cell angles | 90.00, 106.86, 90.00 |
Refinement procedure
Resolution | 19.320 - 2.600 |
R-factor | 0.214 |
Rwork | 0.214 |
R-free | 0.26900 |
Structure solution method | SIRAS |
RMSD bond length | 0.007 |
RMSD bond angle | 1.200 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | SOLVE |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.590 |
High resolution limit [Å] | 2.500 | 2.500 |
Number of reflections | 8118 | |
<I/σ(I)> | 19.7 | 2.2 |
Redundancy | 4.4 | 2.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 277 | 1.8M sodium/potassium phosphate buffer pH8.0, 0.9mM CTAB (Cetyltrimethylammonium Bromide), 5mM DTT, VAPOR DIFFUSION, HANGING DROP, temperature 277K |