2UWC
Crystal structure of Nasturtium xyloglucan hydrolase isoform NXG2
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID23-1 |
Synchrotron site | ESRF |
Beamline | ID23-1 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2006-03-21 |
Detector | ADSC CCD |
Spacegroup name | P 6 |
Unit cell lengths | 152.123, 152.123, 83.233 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 31.310 - 2.300 |
R-factor | 0.168 |
Rwork | 0.167 |
R-free | 0.19600 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1un1 |
RMSD bond length | 0.024 |
RMSD bond angle | 2.103 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | AMoRE |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 45.000 | 2.420 |
High resolution limit [Å] | 2.300 | 2.300 |
Rmerge | 0.110 | 0.600 |
Number of reflections | 47776 | |
<I/σ(I)> | 10.9 | 2.5 |
Completeness [%] | 98.3 | 99.1 |
Redundancy | 4.7 | 4.7 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8.5 | 2-3 M POTASSIUM ACETATE, 2% 2, 5-METHYLPENTANE-DIOL AND 100 MM TRIS BUFFER AT PH 8.5 |