3EI3
Structure of the hsDDB1-drDDB2 complex
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 | 2007-12-15 |
Detector | MARMOSAIC 225 mm CCD |
Wavelength(s) | 0.9918 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 109.440, 114.360, 173.490 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.300 |
R-factor | 0.21 |
Rwork | 0.208 |
R-free | 0.25100 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.205 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | REFMAC (5.4.0066) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 95.350 | 2.400 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.070 | 0.406 |
Number of reflections | 96994 | 11488 |
<I/σ(I)> | 19 | 4.7 |
Completeness [%] | 99.8 | 99.7 |
Redundancy | 6.2 | 6.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.7 | 298 | 100mM Ca-Acetate, 100mM MES pH 5.7, 12-14% PEG 400, VAPOR DIFFUSION, HANGING DROP, temperature 298K |