6JDJ
Crystal structure of AcrIIC2 dimer in complex with partial Nme1Cas9
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 | 2018-03-30 |
| Detector | DECTRIS PILATUS3 S 6M |
| Wavelength(s) | 0.97891 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 61.439, 77.347, 106.885 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 38.673 - 2.600 |
| R-factor | 0.1954 |
| Rwork | 0.194 |
| R-free | 0.22650 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 6jd7 |
| RMSD bond length | 0.005 |
| RMSD bond angle | 0.996 |
| 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 | 2.640 |
| High resolution limit [Å] | 2.600 | 2.600 |
| Rmerge | 0.154 | 0.900 |
| Rmeas | 0.161 | 0.952 |
| Rpim | 0.045 | 0.301 |
| Number of reflections | 16424 | 803 |
| <I/σ(I)> | 2.3 | 2.3 |
| Completeness [%] | 99.9 | 99.4 |
| Redundancy | 12.1 | 9.4 |
| CC(1/2) | 0.995 | 0.815 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | EVAPORATION | 7 | 289 | 0.1M HEPES 7.9, 14% PEG 20000 |






