3LJD
The X-ray structure of zebrafish RNase1 from a new crystal form at pH 4.5
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ELETTRA BEAMLINE 5.2R |
Synchrotron site | ELETTRA |
Beamline | 5.2R |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2008-11-16 |
Detector | MAR CCD 165 mm |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 41.339, 48.971, 109.913 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 30.000 - 1.380 |
R-factor | 0.148 |
Rwork | 0.148 |
R-free | 0.18200 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1agi |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | CNS (1.1) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 30.000 |
High resolution limit [Å] | 1.380 |
Rmerge | 0.049 |
Number of reflections | 41877 |
Completeness [%] | 89.7 |
Redundancy | 3.2 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.5 | 293 | Drops were prepared by mixing equal volumes of protein solution (15 mg/ml) and reservoir solution (2M ammonium sulphate and 0.1M sodium acetate), pH 4.5, VAPOR DIFFUSION, HANGING DROP, temperature 293K |