4F7S
Crystal structure of human CDK8/CYCC in the DMG-in conformation
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SLS BEAMLINE X06SA |
Synchrotron site | SLS |
Beamline | X06SA |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2011-06-08 |
Detector | DECTRIS PILATUS 6M |
Wavelength(s) | 0.90001 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 70.498, 70.774, 170.141 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 85.070 - 2.200 |
R-factor | 0.19354 |
Rwork | 0.193 |
R-free | 0.22193 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3rgf |
RMSD bond length | 0.010 |
RMSD bond angle | 1.178 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | MOLREP |
Refinement software | REFMAC (5.5.0109) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 85.070 | 2.340 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.074 | 0.683 |
Number of reflections | 43856 | |
Completeness [%] | 99.5 | 99.5 |
Redundancy | 5.4 | 5.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.9 | 293.15 | 20% PEG3350, 0.2 M sodium formate, pH 6.9, VAPOR DIFFUSION, HANGING DROP, temperature 293.15K |