1D9Z
CRYSTAL STRUCTURE OF THE DNA REPAIR PROTEIN UVRB IN COMPLEX WITH ATP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | NSLS BEAMLINE X26C |
Synchrotron site | NSLS |
Beamline | X26C |
Temperature [K] | 90 |
Detector technology | CCD |
Collection date | 1999-08-09 |
Detector | ADSC QUANTUM 4 |
Spacegroup name | P 31 2 1 |
Unit cell lengths | 153.443, 153.443, 80.741 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 20.000 - 3.150 |
R-factor | 0.262 * |
Rwork | 0.262 |
R-free | 0.33500 |
RMSD bond length | 0.009 |
RMSD bond angle | 0.031 |
Data scaling software | SCALEPACK |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 3.320 |
High resolution limit [Å] | 3.150 | 3.150 |
Rmerge | 0.140 | 0.520 * |
Number of reflections | 19075 | |
<I/σ(I)> | 17.7 | |
Completeness [%] | 100.0 | 100 |
Redundancy | 6 | 7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 9 | 295 | 8 mg/ml UvrB, 500 mM NaCl, 14-18% PEG 6000, 10 mM ZnCl2, 100 mM Bicine pH 9, pH 9.0, VAPOR DIFFUSION, temperature 295K |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 8 (mg/ml) | |
10 | 1 | reservoir | PEG6000 | 20 (%) | |
11 | 1 | reservoir | 500 (mM) | ||
12 | 1 | reservoir | Tris-HCl | 100 (mM) | |
2 | 1 | drop | 500 (mM) | ||
3 | 1 | drop | Tris-HCl | 20 (mM) | |
4 | 1 | drop | dithiothreitol | 1 (mM) | |
5 | 1 | drop | EDTA | 0.1 (mM) | |
6 | 1 | drop | dodecylmaltoside | 0.03 (%) | |
7 | 1 | drop | PEG6000 | 14-18 (%) | or PEG20000 |
8 | 1 | drop | 10 (mM) | ||
9 | 1 | drop | Bicine | 100 (mM) |