3TA9
beta-Glucosidase A from the halothermophile H. orenii
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 | 2011-03-29 |
Detector | ADSC QUANTUM 315 |
Wavelength(s) | 0.95375 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 88.504, 99.577, 109.427 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 24.894 - 3.000 |
R-factor | 0.1948 |
Rwork | 0.191 |
R-free | 0.26620 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3FJ0 |
RMSD bond length | 0.008 |
RMSD bond angle | 1.230 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.6.4_486)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 74.000 | 3.160 |
High resolution limit [Å] | 3.000 | 3.000 |
Number of reflections | 19515 | |
Completeness [%] | 98.4 | 96 |
Redundancy | 7.9 | 6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 6.5 | 293 | 0.2 M magnesium acetate, 20% PEG8000, 0.1 M sodium cacodylate, pH 6.5, VAPOR DIFFUSION, SITTING DROP, temperature 293K |