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9FVN

Crystal structure of 14-3-3 sigma in complex with Tau pS214 peptide and covalent stabilizer NZ4

This is a non-PDB format compatible entry.
Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsESRF BEAMLINE ID30B
Synchrotron siteESRF
BeamlineID30B
Temperature [K]100
Detector technologyPIXEL
Collection date2023-09-16
DetectorDECTRIS EIGER2 X 9M
Wavelength(s)0.873129
Spacegroup nameC 2 2 21
Unit cell lengths82.203, 111.990, 62.266
Unit cell angles90.00, 90.00, 90.00
Refinement procedure
Resolution56.060 - 1.500
R-factor0.18467
Rwork0.183
R-free0.20883
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.016
RMSD bond angle1.553
Data scaling softwareAimless
Phasing softwareMOLREP
Refinement softwareREFMAC (refmac5)
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]66.2701.530
High resolution limit [Å]1.5001.500
Number of reflections462892240
<I/σ(I)>20.6
Completeness [%]100.0
Redundancy7.8
CC(1/2)0.9990.940
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, SITTING DROP27710mg/mL 14-3-3sigma delta C, 1.5eq peptide, 0.095 M HEPES pH 7.1, 28% PEG400, 0.19 M CaCl2, 5% (v/v) glycerol compound soaked

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