5ANH
CRYSTAL STRUCTURE OF LACCASE FROM BASIDIOMYCETE PM1 (CECT 2971)
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 | 2015-05-08 |
Detector | DECTRIS PILATUS 6M |
Spacegroup name | C 1 2 1 |
Unit cell lengths | 101.440, 175.660, 103.700 |
Unit cell angles | 90.00, 104.16, 90.00 |
Refinement procedure
Resolution | 49.180 - 2.492 |
R-factor | 0.1966 |
Rwork | 0.193 |
R-free | 0.27290 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | PDB ENRY 2HRG |
RMSD bond length | 0.009 |
RMSD bond angle | 1.177 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 2.640 |
High resolution limit [Å] | 2.490 | 2.490 |
Rmerge | 0.120 | 0.480 |
Number of reflections | 59209 | |
<I/σ(I)> | 8.82 | 2.07 |
Completeness [%] | 96.6 | 89 |
Redundancy | 2.97 | 2.91 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 0.1 M TRIS-HCL PH 8.5, 1.6 M AMMONIUM SULFATE, 1.5 M LITHIUM SULFATE |