6VLI
Crystal structure of transcriptional regulator from bacteriophage 186
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX1 |
Synchrotron site | Australian Synchrotron |
Beamline | MX1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-12-05 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.95 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 55.470, 53.510, 106.350 |
Unit cell angles | 90.00, 100.88, 90.00 |
Refinement procedure
Resolution | 54.473 - 2.100 |
R-factor | 0.223080930671 |
Rwork | 0.221 |
R-free | 0.26068 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | SAD model from previous experiments |
RMSD bond length | 0.002 |
RMSD bond angle | 0.483 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | PHENIX (dev_2689) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 54.473 | 2.160 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.248 | 1.492 |
Rmeas | 0.270 | 1.622 |
Rpim | 0.105 | 0.627 |
Number of reflections | 35935 | 2958 |
<I/σ(I)> | 5 | 1.3 |
Completeness [%] | 99.6 | 99.6 |
Redundancy | 6.5 | 6.6 |
CC(1/2) | 0.986 | 0.528 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 8 | 289 | 8% Tascimate pH 8.0, 20% PEG 3350 |