6JGA
Crystal structure of barley exohydrolaseI W286F in complex with 4'-nitrophenyl thiolaminaribioside
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 | 2012-11-22 |
Detector | ADSC QUANTUM 210r |
Wavelength(s) | 0.9537 |
Spacegroup name | P 43 21 2 |
Unit cell lengths | 100.458, 100.458, 181.679 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 36.110 - 1.470 |
R-factor | 0.1535 |
Rwork | 0.153 |
R-free | 0.16850 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3wli |
RMSD bond length | 0.008 |
RMSD bond angle | 1.412 |
Data reduction software | XDS |
Data scaling software | Aimless |
Phasing software | MOLREP |
Refinement software | REFMAC (5.7.0029) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 87.910 | 1.510 |
High resolution limit [Å] | 1.470 | 1.470 |
Rmerge | 0.066 | 0.066 |
Number of reflections | 149209 | 10916 |
<I/σ(I)> | 50.8 | |
Completeness [%] | 99.6 | |
Redundancy | 24 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 277 | 1.7 M ammonium sulfate, 75 mM HEPES-NaOH buffer, pH 7, containing 7.5 mM sodium acetate and 1.2% (w/v) PEG 400 |