4XB4
Structure of the N-terminal domain of OCP binding canthaxanthin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 5.0.2 |
Synchrotron site | ALS |
Beamline | 5.0.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2014-08-28 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 1 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 51.251, 64.112, 53.634 |
Unit cell angles | 90.00, 114.89, 90.00 |
Refinement procedure
Resolution | 38.757 - 1.544 |
R-factor | 0.1479 |
Rwork | 0.147 |
R-free | 0.15990 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | Truncated version of 3MG1 |
RMSD bond length | 0.007 |
RMSD bond angle | 1.042 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX ((phenix.refine: 1.9_1690)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 39.000 | 1.600 |
High resolution limit [Å] | 1.540 | 1.540 |
Rmerge | 0.025 | 0.315 |
Number of reflections | 46069 | |
<I/σ(I)> | 13.8 | 2.52 |
Completeness [%] | 99.5 | 96.33 |
Redundancy | 7.2 | 2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, SITTING DROP | 295 | 100 mM citric acid BIS-TRIS propane pH 5.5, 24% poly-ethylene glycol 3350 |