3IQI
Structure of O-Acetylserine Sulfhydrylase in Complex with Peptide MNENI
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | ROTATING ANODE |
Source details | RIGAKU RUH3R |
Temperature [K] | 130 |
Detector technology | IMAGE PLATE |
Collection date | 2009-01-16 |
Detector | RIGAKU RAXIS IV++ |
Wavelength(s) | 1.5418 |
Spacegroup name | I 41 |
Unit cell lengths | 112.264, 112.264, 45.835 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 22.080 - 1.700 |
R-factor | 0.1737 |
Rwork | 0.172 |
R-free | 0.20439 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1y7l |
RMSD bond length | 0.011 |
RMSD bond angle | 1.282 |
Data reduction software | MOSFLM |
Data scaling software | SCALA |
Phasing software | REFMAC |
Refinement software | REFMAC |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 22.080 | 1.790 |
High resolution limit [Å] | 1.700 | 1.700 |
Rmerge | 0.033 | 0.152 |
Number of reflections | 29196 | |
<I/σ(I)> | 28.1 | 6.2 |
Completeness [%] | 97.3 | 85.9 |
Redundancy | 3.3 | 3 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7.5 | 298 | HEPES, Ammonium sulfate, PEG 400, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K |