1H55
STRUCTURE OF HORSERADISH PEROXIDASE C1A COMPOUND II
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE BM14 |
Synchrotron site | ESRF |
Beamline | BM14 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 1999-06-15 |
Detector | MARRESEARCH |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 40.243, 67.421, 117.291 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 33.180 - 1.610 |
R-factor | 0.188 |
Rwork | 0.188 |
R-free | 0.21000 |
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] | 33.200 | 1.650 |
High resolution limit [Å] | 1.610 | 1.610 |
Rmerge | 0.105 | 0.366 |
Number of reflections | 40391 | |
<I/σ(I)> | 9.5 | 4 |
Completeness [%] | 95.5 | 94.9 |
Redundancy | 2.93 |
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 |