5CDX
Crystal structure of conserpin
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | AUSTRALIAN SYNCHROTRON BEAMLINE MX2 |
Synchrotron site | Australian Synchrotron |
Beamline | MX2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-12-16 |
Detector | ADSC QUANTUM 315r |
Wavelength(s) | 0.953690 |
Spacegroup name | C 2 2 21 |
Unit cell lengths | 68.140, 76.120, 150.240 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 42.060 - 2.400 |
R-factor | 0.1975 |
Rwork | 0.194 |
R-free | 0.25820 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3ne4 |
RMSD bond length | 0.007 |
RMSD bond angle | 1.025 |
Data scaling software | SCALA |
Phasing software | PHASER |
Refinement software | PHENIX (1.7.3_928) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 42.060 | 2.486 |
High resolution limit [Å] | 2.400 | 2.400 |
Rmerge | 0.045 | |
Number of reflections | 15325 | |
<I/σ(I)> | 9.2 | 2.16 |
Completeness [%] | 97.8 | 97.46 |
Redundancy | 2 | 2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 288 | Crystals appeared within 5 days in 0.2 M magnesium chloride hexahydrate, 16% PEG-3350, 10 mM bis-tris, pH 7.5 |