5D39
Transcription factor-DNA complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 21-ID-D |
Synchrotron site | APS |
Beamline | 21-ID-D |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2015-06-22 |
Detector | MAR scanner 300 mm plate |
Wavelength(s) | 0.98 |
Spacegroup name | P 1 |
Unit cell lengths | 68.395, 94.697, 145.642 |
Unit cell angles | 79.62, 78.31, 89.58 |
Refinement procedure
Resolution | 44.120 - 3.200 |
R-factor | 0.2111 |
Rwork | 0.210 |
R-free | 0.23610 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4y5u |
RMSD bond length | 0.006 |
RMSD bond angle | 1.321 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 44.120 | 3.260 |
High resolution limit [Å] | 3.200 | 3.200 |
Rmerge | 0.082 | 0.695 |
Number of reflections | 57110 | |
<I/σ(I)> | 16.7 | |
Completeness [%] | 99.0 | 98.9 |
Redundancy | 3.4 | 3.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 289 | 0.1 M citrate (pH 5.6), 0.1 M NaCl, 20% isopropyl alcohol and 8% PEG4000 |