7QAZ
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 | 2021-08-07 |
Detector | DECTRIS EIGER2 XE 16M |
Wavelength(s) | 0.9795 |
Spacegroup name | P 21 21 21 |
Unit cell lengths | 227.910, 39.620, 79.770 |
Unit cell angles | 90.00, 90.00, 90.00 |
Refinement procedure
Resolution | 56.980 - 2.110 |
R-factor | 0.2123 |
Rwork | 0.210 |
R-free | 0.26080 |
Structure solution method | MOLECULAR REPLACEMENT |
Starting model (for MR) | 7nqe |
RMSD bond length | 0.007 |
RMSD bond angle | 0.979 |
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] | 56.980 | 2.150 |
High resolution limit [Å] | 2.110 | 2.110 |
Rmerge | 0.151 | 1.042 |
Rmeas | 0.174 | 1.382 |
Rpim | 0.085 | 0.896 |
Number of reflections | 40376 | 1427 |
<I/σ(I)> | 6.5 | 0.6 |
Completeness [%] | 94.4 | 69.6 |
Redundancy | 3.8 | 1.9 |
CC(1/2) | 0.992 | 0.298 |
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 400uM DNA; 500uM AMPNPP; 4mM GTP; 2mM CoCl2; 130mM Monopotassium Glutamate |