2XLK
Crystal structure of the Csy4-crRNA complex, orthorhombic form
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | ALS BEAMLINE 8.2.2 |
Synchrotron site | ALS |
Beamline | 8.2.2 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-04-18 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 40.060, 78.910, 145.940 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 69.413 - 1.805 |
R-factor | 0.186 |
Rwork | 0.184 |
R-free | 0.21600 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 2xli |
RMSD bond length | 0.006 |
RMSD bond angle | 1.086 |
Data reduction software | XDS |
Data scaling software | XSCALE |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 69.400 | 1.900 |
High resolution limit [Å] | 1.800 | 1.800 |
Rmerge | 0.070 | 0.530 |
Number of reflections | 43284 | |
<I/σ(I)> | 31.1 | 3.1 |
Completeness [%] | 98.7 | 91 |
Redundancy | 19.8 | 6.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 4.6 | 160 MM SODIUM ACETATE PH 4.6, 18% (W/V) PEG 4000 |