4ILM
CRISPR RNA Processing endoribonuclease
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | APS BEAMLINE 22-ID |
Synchrotron site | APS |
Beamline | 22-ID |
Temperature [K] | 100 |
Detector technology | IMAGE PLATE |
Collection date | 2012-04-21 |
Detector | MAR scanner 300 mm plate |
Wavelength(s) | 0.9792 |
Spacegroup name | P 1 21 1 |
Unit cell lengths | 78.981, 154.608, 130.848 |
Unit cell angles | 90.00, 93.64, 90.00 |
Refinement procedure
Resolution | 35.000 - 3.068 |
R-factor | 0.2346 |
Rwork | 0.233 |
R-free | 0.28400 |
Structure solution method | MOLECULAR REPLACEMENT |
RMSD bond length | 0.006 |
RMSD bond angle | 1.229 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASES |
Refinement software | PHENIX ((phenix.refine: 1.8_1069)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 35.000 | 3.100 |
High resolution limit [Å] | 3.000 | 3.000 |
Number of reflections | 57752 | |
<I/σ(I)> | 24.9 | |
Completeness [%] | 95.9 | 70.6 |
Redundancy | 6.7 | 3.4 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | VAPOR DIFFUSION, HANGING DROP | 7 | 303 | 15%(v/v) isopropanol, 1mM spermine, 10mM Co(NH4)6Cl3, 50mM Tris-HCl (pH 7.0), VAPOR DIFFUSION, HANGING DROP, temperature 303K |