3HY5
Crystal structure of CRALBP
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ESRF BEAMLINE ID29 |
Synchrotron site | ESRF |
Beamline | ID29 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2007-11-06 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.97618 |
Spacegroup name | P 65 2 2 |
Unit cell lengths | 71.930, 71.930, 303.160 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 48.130 - 3.040 |
R-factor | 0.242 |
Rwork | 0.239 |
R-free | 0.27200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3hx3 |
RMSD bond length | 0.004 |
RMSD bond angle | 0.741 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.220 |
High resolution limit [Å] | 3.040 | 3.040 |
Rmerge | 0.059 | 0.534 |
Number of reflections | 9692 | 1499 |
<I/σ(I)> | 22.8 | 4.1 |
Completeness [%] | 99.5 | 99.6 |
Redundancy | 10.6 | 9.6 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION | 7 | 298 | 1M Sodium-potassium tartrate, 0.2M Lithium sulfate, pH 7.0, VAPOR DIFFUSION, temperature 298K |