1LQM
ESCHERICHIA COLI URACIL-DNA GLYCOSYLASE COMPLEX WITH URACIL-DNA GLYCOSYLASE INHIBITOR PROTEIN
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RU200 |
Temperature [K] | 293 |
Detector technology | IMAGE PLATE |
Detector | MARRESEARCH |
Wavelength(s) | 1.5418 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 98.757, 158.875, 91.222 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 15.000 - 3.200 |
R-factor | 0.188 |
Rwork | 0.188 |
R-free | 0.26000 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1uug |
RMSD bond length | 0.011 |
RMSD bond angle | 26.400 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | AMoRE |
Refinement software | X-PLOR (3.851) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 3.310 |
High resolution limit [Å] | 3.200 | 3.200 |
Rmerge | 0.167 * | 0.398 * |
Total number of observations | 94765 * | |
Number of reflections | 21106 | |
<I/σ(I)> | 9.2 | 1.4 |
Completeness [%] | 87.6 | 79.3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.6 | 281 * | 20mM imidazole-maleate, 10% PEG 4000, pH 7.6, VAPOR DIFFUSION, HANGING DROP at 293K, temperature 293.0K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 10 (mg/ml) | |
2 | 1 | drop | imidazole malate | 20 (mM) | pH7.6 |
3 | 1 | reservoir | PEG4000 | 10 (%(w/v)) |