1H5A
STRUCTURE OF FERRIC HORSERADISH PEROXIDASE C1A IN COMPLEX WITH ACETATE
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID14-3 |
Synchrotron site | ESRF |
Beamline | ID14-3 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 1999-02-15 |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 40.347, 67.774, 117.265 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 19.710 - 1.600 |
R-factor | 0.178 |
Rwork | 0.178 |
R-free | 0.20200 |
Structure solution method | OTHER |
RMSD bond length | 0.005 |
RMSD bond angle | 1.200 |
Data reduction software | DENZO |
Data scaling software | SCALEPACK |
Phasing software | CNS |
Refinement software | CNS (1.0) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 19.700 | 1.640 |
High resolution limit [Å] | 1.600 | 1.600 |
Rmerge | 0.058 | 0.203 |
Number of reflections | 42167 | |
<I/σ(I)> | 18.2 | 6.8 |
Completeness [%] | 97.7 | 93.9 |
Redundancy | 4.36 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 6.5 | 20% (W/V) PEG 4000, 0.2 M CALCIUM ACETATE, 0.1 M CACODYLATE BUFFER, PH 6.5 |