2E3W
X-ray structure of native RNase A
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 77 |
Detector technology | CCD |
Collection date | 2006-08-15 |
Detector | MARMOSAIC 300 mm CCD |
Wavelength(s) | 0.90020 |
Spacegroup name | P 32 2 1 |
Unit cell lengths | 64.167, 64.167, 63.626 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 20.000 - 1.050 |
R-factor | 0.19329 |
Rwork | 0.193 |
R-free | 0.20783 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 1izp |
RMSD bond length | 0.014 |
RMSD bond angle | 1.570 |
Refinement software | REFMAC (5.2.0019) |
Data quality characteristics
Overall | |
Low resolution limit [Å] | 50.000 |
High resolution limit [Å] | 1.050 |
Number of reflections | 69871 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 5.89 | 292 | Well solution: Combination of Hampton Index Reagents 3 and 9, Final solution: 0.1 M Bis-tris, 1.0 M ammonium sulfate, 1.5 M NaCl, pH 5.89, Drop: 2 microliter well solution + 2 microliter 10 mg/ml protein solution in water, VAPOR DIFFUSION, HANGING DROP, temperature 292K |