1ODG
Very-short-patch DNA repair endonuclease bound to its reaction product site
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2000-02-15 |
Detector | ADSC CCD |
Spacegroup name | P 61 |
Unit cell lengths | 102.805, 102.805, 64.290 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 24.700 - 2.800 |
R-factor | 0.2873 |
Rwork | 0.287 |
R-free | 0.35600 * |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1cw0 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.306 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.900 |
High resolution limit [Å] | 2.750 | 2.750 |
Rmerge | 0.070 | 0.384 |
Number of reflections | 10084 | 1464 * |
<I/σ(I)> | 6.9 | 2 |
Completeness [%] | 99.0 | 100 |
Redundancy | 4.9 | 5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Batch method * | 6.5 | 14 * | 25 MM HEPES PH7.0, 75 MM NACL, 15% PEG 8000, 50 MM SODIUM CACODYLATE PH 6.5, 75 MM AMMONIUM SULPHATE AND 10% GLYCEROL PROTEIN 2.5 MG/ML |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | 1 | HEPES | 25 (mM) | pH7.0 |
2 | 1 | 1 | 75 (mM) | ||
3 | 1 | 1 | PEG8000 | 15 (%) | |
4 | 1 | 1 | sodium cacodylate | 50 (mM) | pH6.5 |
5 | 1 | 1 | ammonium sulfate | 75 (mM) | |
6 | 1 | 1 | glycerol | 10 (%) | |
7 | 1 | 1 | protein | 2.5 (mg/ml) |