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7P9J

Prim-Pol Domain of CRISPR-associated Prim-Pol (CAPP) from Marinitoga sp. 1137 - Primer Initiation Complex

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsDIAMOND BEAMLINE I04
Synchrotron siteDiamond
BeamlineI04
Temperature [K]100
Detector technologyPIXEL
Collection date2021-05-14
DetectorDECTRIS EIGER2 XE 16M
Wavelength(s)0.9795
Spacegroup nameP 21 21 21
Unit cell lengths227.820, 39.500, 74.980
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution45.350 - 1.900
R-factor0.2291
Rwork0.228
R-free0.25900
Structure solution methodMOLECULAR REPLACEMENT
Starting model (for MR)7nqd
RMSD bond length0.009
RMSD bond angle1.347
Data reduction softwarexia2 (3.4.2)
Data scaling softwareXSCALE
Phasing softwarePHASER (2.8.3)
Refinement softwarePHENIX (1.19.2_4158)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]45.3501.930
High resolution limit [Å]1.9001.900
Rmerge0.0701.373
Rmeas0.0871.777
Rpim0.0511.112
Number of reflections417622100
<I/σ(I)>7.70.5
Completeness [%]76.478.2
Redundancy2.52.1
CC(1/2)0.9970.282
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP7.5287.150.1M 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

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