7P9J
Prim-Pol Domain of CRISPR-associated Prim-Pol (CAPP) from Marinitoga sp. 1137 - Primer Initiation Complex
Experimental procedure
| Experimental method | SINGLE WAVELENGTH |
| Source type | SYNCHROTRON |
| Source details | DIAMOND BEAMLINE I04 |
| Synchrotron site | Diamond |
| Beamline | I04 |
| Temperature [K] | 100 |
| Detector technology | PIXEL |
| Collection date | 2021-05-14 |
| Detector | DECTRIS EIGER2 XE 16M |
| Wavelength(s) | 0.9795 |
| Spacegroup name | P 21 21 21 |
| Unit cell lengths | 227.820, 39.500, 74.980 |
| Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
| Resolution | 45.350 - 1.900 |
| R-factor | 0.2291 |
| Rwork | 0.228 |
| R-free | 0.25900 |
| Structure solution method | MOLECULAR REPLACEMENT |
| Starting model (for MR) | 7nqd |
| RMSD bond length | 0.009 |
| RMSD bond angle | 1.347 |
| Data reduction software | xia2 (3.4.2) |
| Data scaling software | XSCALE |
| Phasing software | PHASER (2.8.3) |
| Refinement software | PHENIX (1.19.2_4158) |
Data quality characteristics
| Overall | Outer shell | |
| Low resolution limit [Å] | 45.350 | 1.930 |
| High resolution limit [Å] | 1.900 | 1.900 |
| Rmerge | 0.070 | 1.373 |
| Rmeas | 0.087 | 1.777 |
| Rpim | 0.051 | 1.112 |
| Number of reflections | 41762 | 2100 |
| <I/σ(I)> | 7.7 | 0.5 |
| Completeness [%] | 76.4 | 78.2 |
| Redundancy | 2.5 | 2.1 |
| CC(1/2) | 0.997 | 0.282 |
Crystallization Conditions
| crystal ID | method | pH | temperature | details |
| 1 | VAPOR DIFFUSION, SITTING DROP | 7.5 | 287.15 | 0.1M Sodium HEPES; MOPS (acid) 20% v/v Ethylene glycol; 10% w/v PEG 8000 0.03M Diethylene glycol; 0.03M Triethylene glycol; 0.03M Tetraethylene glycol; 0.03M Pentaethylene glycol 200uM DNA; 500uM AMPNPP; 2mM GTP; 2mM CoCl2; 140mM Monopotassium Glutamate |






