5LSV
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 | 2013-05-21 |
Detector | MAR CCD 165 mm |
Wavelength(s) | 1.0000 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 45.400, 58.840, 71.900 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.000 - 1.100 |
R-factor | 0.10164 |
Rwork | 0.101 |
R-free | 0.12451 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4opb |
RMSD bond length | 0.022 |
RMSD bond angle | 2.038 |
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 | 1.130 |
High resolution limit [Å] | 1.100 | 1.100 |
Rmeas | 0.129 | 0.900 |
Number of reflections | 78799 | |
<I/σ(I)> | 13.37 | |
Completeness [%] | 99.9 | 99.9 |
Redundancy | 7.44 | 6.76 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5 | 298 | 20%(v/v)PEG3000 0.2M Zn-acetate 0.1 M Malate/MES/Tris pH5.0 |