3FEF
Crystal structure of putative glucosidase lplD from bacillus subtilis
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 24-ID-C |
Synchrotron site | APS |
Beamline | 24-ID-C |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-11-05 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.979 |
Spacegroup name | P 1 |
Unit cell lengths | 81.987, 84.843, 86.051 |
Unit cell angles | 69.80, 68.10, 64.07 |
Refinement procedure
Resolution | 50.000 - 2.200 |
R-factor | 0.19 |
Rwork | 0.187 |
R-free | 0.24300 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.249 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | PHENIX |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.280 |
High resolution limit [Å] | 2.200 | 2.200 |
Rmerge | 0.070 | 0.174 |
Number of reflections | 90052 | |
<I/σ(I)> | 10.697 | 5.1 |
Completeness [%] | 94.0 | 63.8 |
Redundancy | 2.9 | 1.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 7 | 298 | 23% PEG 3350, 0.17M Ammonium Sulphate, 0.1M Magnesium Acetate, pH 7.0, Vapor diffusion, Sitting drop, temperature 298K |