7D88
Crystal structure of a novel thermostable GH10 xylanase XynA
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 298 |
Detector technology | CCD |
Collection date | 2019-03-20 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.979 |
Spacegroup name | P 41 2 2 |
Unit cell lengths | 109.842, 109.842, 85.570 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 15.326 - 2.345 |
R-factor | 0.216210592416 |
Rwork | 0.214 |
R-free | 0.24829 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1v0l |
RMSD bond length | 0.008 |
RMSD bond angle | 0.965 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHENIX |
Refinement software | PHENIX (1.11.1_2575) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.330 | 2.429 |
High resolution limit [Å] | 2.300 | 2.345 |
Rmerge | 0.158 | |
Rmeas | 0.159 | |
Rpim | 0.031 | |
Number of reflections | 22405 | 22405 |
<I/σ(I)> | 30 | |
Completeness [%] | 99.3 | |
Redundancy | 25.3 | |
CC(1/2) | 0.990 | 0.990 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 6 | 298 | 29% PEG 600 (w/v), 0.1 M CaCl2, 0.1 M MES pH 6.0 |