7AYP
Structure of a GH11 domain refined from the X-ray diffraction data of a GH11-CBM36-1 crystal.
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2016-12-14 |
Detector | DECTRIS PILATUS 6M-F |
Wavelength(s) | 0.65 |
Spacegroup name | P 63 |
Unit cell lengths | 108.216, 108.216, 54.228 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 54.108 - 1.700 |
R-factor | 0.171746959432 |
Rwork | 0.171 |
R-free | 0.18689 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2dcj |
RMSD bond length | 0.006 |
RMSD bond angle | 0.934 |
Refinement software | PHENIX (1.12_2829) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 93.690 | 3.900 |
High resolution limit [Å] | 1.470 | 1.470 |
Number of reflections | 65364 | 3225 |
<I/σ(I)> | 15.81 | |
Completeness [%] | 99.9 | 99 |
Redundancy | 1 | |
CC(1/2) | 0.999 | 0.814 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 4.8 | 293.16 | Na acetate, (NH4)2SO4 |