2Q2E
Crystal structure of the topoisomerase VI holoenzyme from Methanosarcina mazei
Experimental procedure
Experimental method | MAD |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.3.1 |
Synchrotron site | ALS |
Beamline | 8.3.1 |
Temperature [K] | 80 |
Detector technology | CCD |
Collection date | 2006-03-01 |
Detector | ADSC QUANTUM 210 |
Wavelength(s) | 1.1159, 1.2386, 1.21495, 1.21434 |
Spacegroup name | P 64 2 2 |
Unit cell lengths | 227.812, 227.812, 208.660 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 30.000 - 4.000 |
R-factor | 0.3079 |
Rwork | 0.306 |
R-free | 0.34927 |
Structure solution method | MAD |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MLPHARE |
Refinement software | REFMAC (5.3.0026) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 100.000 | 4.220 |
High resolution limit [Å] | 4.000 | 4.000 |
Number of reflections | 25975 | |
<I/σ(I)> | 9.1 | 1.8 |
Completeness [%] | 95.2 | 96.8 |
Redundancy | 5 | 4.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6 | 292 | 100 mM sodium cacodylate pH 6.0, 1.6-1.8 M ammonium sulfate pH 7.5, 10 mM magnesium chloride, 10 20% glycerol, VAPOR DIFFUSION, HANGING DROP, temperature 292K |