6JDV
Crystal structure of Nme1Cas9 in complex with sgRNA and target DNA (ATATGATT PAM) in catalytic state
Experimental procedure
Experimental method | SINGLE WAVELENGTH |
Source type | SYNCHROTRON |
Source details | SSRF BEAMLINE BL19U1 |
Synchrotron site | SSRF |
Beamline | BL19U1 |
Temperature [K] | 100 |
Detector technology | PIXEL |
Collection date | 2018-01-15 |
Detector | DECTRIS PILATUS3 S 6M |
Wavelength(s) | 0.9786 |
Spacegroup name | P 21 21 2 |
Unit cell lengths | 130.541, 158.340, 118.253 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 41.958 - 3.100 |
R-factor | 0.2132 |
Rwork | 0.212 |
R-free | 0.23140 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 5x2g |
RMSD bond length | 0.013 |
RMSD bond angle | 1.209 |
Data reduction software | HKL-2000 |
Data scaling software | HKL-2000 |
Phasing software | PHASER |
Refinement software | PHENIX ((1.14_3247: ???)) |
Data quality characteristics
Overall | Outer shell | |
Low resolution limit [Å] | 50.000 | 3.150 |
High resolution limit [Å] | 3.100 | 3.100 |
Rmerge | 0.179 | 0.888 |
Rmeas | 0.193 | 0.951 |
Rpim | 0.070 | 0.336 |
Number of reflections | 45911 | 2234 |
<I/σ(I)> | 11.7 | 2.3 |
Completeness [%] | 99.8 | 99.6 |
Redundancy | 7.4 | 7.7 |
CC(1/2) | 0.987 | 0.904 |
Crystallization Conditions
crystal ID | method | pH | temperature | details |
1 | EVAPORATION | 8 | 289 | Na citrate, 0.1M HEPES pH 8.0, 18.5% PEG 3350 |