2NOJ
Crystal structure of Ehp / C3d complex
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 93 |
Detector technology | CCD |
Collection date | 2006-06-16 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.91840 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 67.894, 91.025, 122.595 |
Unit cell angles | 90.00, 89.93, 90.00 |
Refinement procedure
Resolution | 50.000 - 2.700 |
R-factor | 0.29 |
Rwork | 0.291 |
R-free | 0.28400 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2gox |
RMSD bond length | 0.010 |
RMSD bond angle | 1.337 |
Data reduction software | DENZO |
Data scaling software | HKL-2000 |
Phasing software | MOLREP |
Refinement software | REFMAC (5.2.0005) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 2.699 |
Rmerge | 0.189 |
Number of reflections | 33242 |
Completeness [%] | 80.8 |
Redundancy | 2.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8.2 | 293 | 0.2M LiSO4, 25% PEG 3350, 0.1M Tris-HCl pH 8.2, additive: CaCl2, VAPOR DIFFUSION, HANGING DROP, temperature 293K |