1XEW
Structural biochemistry of ATP-driven dimerization and DNA stimulated activation of SMC ATPases.
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2003-09-09 |
Detector | ADSC QUANTUM 210 |
Wavelength(s) | 0.97913, 0.97931, 0.97121, 0.91677 |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 102.285, 56.744, 78.869 |
Unit cell angles | 90.00, 123.05, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.000 |
Rwork | 0.207 |
R-free | 0.26100 |
Structure solution method | MAD |
RMSD bond length | 0.019 |
RMSD bond angle | 2.300 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | SnB |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 40.000 | 2.050 |
High resolution limit [Å] | 2.000 | 2.000 |
Number of reflections | 22600 | |
Completeness [%] | 88.3 | 55.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 8 | 293 | PEG 8000, glycerol, KCl, VAPOR DIFFUSION, HANGING DROP, temperature 293K |