5T7N
X-ray crystal structure of AA13 LPMO
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | MAX II BEAMLINE I911-3 |
Synchrotron site | MAX II |
Beamline | I911-3 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2013-11-07 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 0.9999 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 45.670, 59.000, 72.150 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.000 - 1.600 |
R-factor | 0.10804 |
Rwork | 0.106 |
R-free | 0.17241 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4opb |
RMSD bond length | 0.018 |
RMSD bond angle | 1.681 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Refinement software | REFMAC (5.8.0073) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 30.000 | 1.640 |
High resolution limit [Å] | 1.600 | 1.600 |
Rmeas | 0.075 | 0.456 |
Number of reflections | 26328 | |
<I/σ(I)> | 3.14 | |
Completeness [%] | 99.7 | 96.9 |
Redundancy | 6.38 | 3.74 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5 | 298 | 20%(v/v)PEG3000 0.2M Zn-acetate 0.1M Malate/MES/TRIS pH5.0 |