3ZQ4
Unusual, dual endo- and exo-nuclease activity in the degradosome explained by crystal structure analysis of RNase J1
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | DIAMOND BEAMLINE I04 |
Synchrotron site | Diamond |
Beamline | I04 |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2010-01-25 |
Detector | ADSC CCD |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 177.823, 209.430, 74.106 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 29.760 - 3.000 |
R-factor | 0.216 |
Rwork | 0.214 |
R-free | 0.25800 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 3bk1 |
RMSD bond length | 0.010 |
RMSD bond angle | 1.324 |
Data reduction software | XDS |
Data scaling software | XDS |
Phasing software | PHASER |
Refinement software | PHENIX ((PHENIX.REFINE: 1.5_2)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 20.000 | 3.160 |
High resolution limit [Å] | 3.000 | 3.000 |
Rmerge | 0.100 | 0.550 |
Number of reflections | 55920 | |
<I/σ(I)> | 11.4 | 2.2 |
Completeness [%] | 98.2 | 98.9 |
Redundancy | 3.5 | 3.5 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | 8 | 0.2 M CACL2, 0.1 M TRIS.HCL, PH 8.0, 10 % (W/V) PEG 6000 |