5TA1
Crystal structure of BuGH86wt
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | CLSI BEAMLINE 08ID-1 |
Synchrotron site | CLSI |
Beamline | 08ID-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-12-07 |
Detector | RAYONIX MX-300 |
Wavelength(s) | 0.97949 |
Spacegroup name | I 2 3 |
Unit cell lengths | 167.660, 167.660, 167.660 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 118.550 - 2.300 |
R-factor | 0.1706 |
Rwork | 0.168 |
R-free | 0.21190 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4aw7 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.340 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0135) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 118.550 | 2.420 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.109 | 0.566 |
Number of reflections | 34836 | |
<I/σ(I)> | 14.8 | 4.7 |
Completeness [%] | 100.0 | 100 |
Redundancy | 11.2 | 11.2 |
CC(1/2) | 0.997 | 0.916 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 291 | 0.16 M CaOAc, 0.08 M Na cacodylate, 14.4% PEG 3350, 20% glycerol |