5MSX
Glycoside hydrolase BT_3662
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I02 |
Synchrotron site | Diamond |
Beamline | I02 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2014-02-14 |
Detector | DECTRIS PILATUS3 6M |
Wavelength(s) | 0.979 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 76.827, 129.181, 158.080 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 49.440 - 2.100 |
R-factor | 0.18931 |
Rwork | 0.187 |
R-free | 0.23468 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3qz4 |
RMSD bond length | 0.011 |
RMSD bond angle | 1.502 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | PHASER |
Refinement software | REFMAC (5.8.0155) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 49.440 | 2.140 |
High resolution limit [Å] | 2.100 | 2.100 |
Rmerge | 0.641 | |
Number of reflections | 91827 | |
<I/σ(I)> | 7.5 | 2.2 |
Completeness [%] | 99.4 | 98.2 |
Redundancy | 3.8 | 4 |
CC(1/2) | 0.711 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 293 | 20% polyethylene glycol (PEG) 6000 and 0.1 M hepes pH 6.5 |