1B8D
CRYSTAL STRUCTURE OF A PHYCOUROBILIN-CONTAINING PHYCOERYTHRIN
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | EMBL/DESY, HAMBURG BEAMLINE X11 |
Synchrotron site | EMBL/DESY, HAMBURG |
Beamline | X11 |
Temperature [K] | 289 |
Detector technology | IMAGE PLATE |
Collection date | 1993-11 |
Detector | MARRESEARCH |
Spacegroup name | H 3 |
Unit cell lengths | 187.350, 187.350, 59.310 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 100.000 - 1.900 |
Rwork | 0.175 |
R-free | 0.22700 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1cpc |
RMSD bond length | 0.004 |
RMSD bond angle | 17.700 * |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | X-PLOR |
Refinement software | X-PLOR (3.843) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 15.000 | 2.000 |
High resolution limit [Å] | 1.820 | 1.820 |
Rmerge | 0.059 | 0.313 |
Total number of observations | 131195 * | |
Number of reflections | 67598 | 15857 * |
Completeness [%] | 96.8 * | 92 |
Redundancy | 1.9 | 1.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | other * | 7.5 | .refer to Ritter, S., (1997) Protein Peptide Lett., 4, 69. * |