4G3A
Crystal Structure of MAST/Orbit N-terminal domain
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 4.2.2 |
Synchrotron site | ALS |
Beamline | 4.2.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2009-12-16 |
Detector | NOIR-1 |
Wavelength(s) | 1.0 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 36.180, 97.579, 149.346 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 48.789 - 1.994 |
R-factor | 0.1897 |
Rwork | 0.188 |
R-free | 0.22860 |
Structure solution method | FOURIER SYNTHESIS |
RMSD bond length | 0.007 |
RMSD bond angle | 1.014 |
Refinement software | PHENIX ((phenix.refine: 1.6_289)) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 82.000 |
High resolution limit [Å] | 1.994 |
Rmerge | 0.059 |
Number of reflections | 36131 |
<I/σ(I)> | 28.9 |
Completeness [%] | 97.4 |
Redundancy | 5.8 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 6.5 | 293 | 12.5% PEG 4000, 0.1M Bis-Tris, 0.1M NaCl & 20% v/v glycerol with a 1:1 ratio of protein to precipitant, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K |