4G05
The crystal structures of several mutants of Pleurotus eryngii versatile peroxidase
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-2 |
Synchrotron site | ESRF |
Beamline | ID14-2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-04-21 |
Detector | ADSC QUANTUM 4r |
Wavelength(s) | 0.933 |
Spacegroup name | I 41 |
Unit cell lengths | 96.430, 96.430, 98.780 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 69.000 - 2.350 |
R-factor | 0.17375 |
Rwork | 0.171 |
R-free | 0.21859 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2vka |
RMSD bond length | 0.021 |
RMSD bond angle | 2.467 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | MOLREP |
Refinement software | REFMAC (5.6.0117) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 69.000 | 2.480 |
High resolution limit [Å] | 2.350 | 2.350 |
Rmerge | 0.180 | 0.454 |
Number of reflections | 18856 | |
<I/σ(I)> | 3.9 | 1.6 |
Completeness [%] | 100.0 | 100 |
Redundancy | 4.1 | 4.1 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 5 | 295 | 1.4 M AMMONIUM SULFATE, 0.1 M SODIUM CACODYLATE, PH 5.0, VAPOR DIFFUSION, SITTING DROP, temperature 295K |