5H1O
CRISPR-associated protein
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | PAL/PLS BEAMLINE 7A (6B, 6C1) |
Synchrotron site | PAL/PLS |
Beamline | 7A (6B, 6C1) |
Temperature [K] | 100 |
Detector technology | CCD |
Collection date | 2016-05-31 |
Detector | ADSC QUANTUM 270 |
Wavelength(s) | 0.9793 |
Spacegroup name | P 63 |
Unit cell lengths | 90.385, 90.385, 50.831 |
Unit cell angles | 90.00, 90.00, 120.00 |
Refinement procedure
Resolution | 29.585 - 1.650 |
R-factor | 0.1683 |
Rwork | 0.166 |
R-free | 0.20520 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 4es2 |
RMSD bond length | 0.013 |
RMSD bond angle | 1.413 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX (1.9_1692) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 1.710 |
High resolution limit [Å] | 1.650 | 1.650 |
Rmerge | 0.071 | 0.809 |
Number of reflections | 28581 | |
<I/σ(I)> | 12.6 | 3.1 |
Completeness [%] | 99.7 | 100 |
Redundancy | 12.1 | 11.5 |
CC(1/2) | 0.899 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 293 | 50mM Ammonium acetate, 85mM Sodium acetate pH 4.6, 23%(w/v) PEG4000. 10%(v/v) Glycerol |