1BG1
TRANSCRIPTION FACTOR STAT3B/DNA COMPLEX
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID2 |
Synchrotron site | ESRF |
Beamline | ID2 |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 1997-10-15 |
Detector | MARRESEARCH |
Spacegroup name | I 41 |
Unit cell lengths | 174.000, 174.000, 79.400 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 20.000 - 2.250 |
R-factor | 0.246 * |
Rwork | 0.246 |
R-free | 0.30100 |
Structure solution method | MULTIPLE ISOMORPHOUS REPLACEMENT |
RMSD bond length | 0.012 |
RMSD bond angle | 21.300 * |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | MLPHARE |
Refinement software | X-PLOR (3.1) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 2.330 |
High resolution limit [Å] | 2.250 | 2.250 |
Rmerge | 0.053 | 0.300 |
Total number of observations | 273455 * | |
Number of reflections | 56005 | |
<I/σ(I)> | 16.4 | |
Completeness [%] | 99.4 | 99.3 |
Redundancy | 4.9 | 3.9 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | Vapor diffusion, hanging drop * | 7 | protein-DNA solution was mixed with an equal volume of reservoir solution * |
Crystallization Reagents in Literatures
ID | crystal ID | solution | reagent name | concentration (unit) | details |
1 | 1 | drop | protein | 0.074 (mM) | |
10 | 1 | reservoir | MES | 50 (mM) | |
11 | 1 | reservoir | ammonium acetate | 0.1 (M) | |
12 | 1 | reservoir | glycerol | 10 (%(v/v)) | |
2 | 1 | drop | HEPES | 20 (mM) | |
3 | 1 | drop | 200 (mM) | ||
4 | 1 | drop | 10 (mM) | ||
5 | 1 | drop | dithiothreitol | 5 (mM) | |
6 | 1 | drop | PMSF | 0.5 (mM) | |
7 | 1 | drop | DNA duplex | ||
8 | 1 | reservoir | 0.1-0.4 (M) | ||
9 | 1 | reservoir | 5 (mM) |