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8FWL

Crystal structure of Australian bat lyssavirus nucleoprotein in complex with phosphoprotein chaperone

Experimental procedure
Experimental methodSINGLE WAVELENGTH
Source typeSYNCHROTRON
Source detailsAUSTRALIAN SYNCHROTRON BEAMLINE MX2
Synchrotron siteAustralian Synchrotron
BeamlineMX2
Temperature [K]100
Detector technologyPIXEL
Collection date2022-06-26
DetectorDECTRIS EIGER X 16M
Wavelength(s)0.9537
Spacegroup nameP 1 2 1
Unit cell lengths82.373, 35.503, 89.091
Unit cell angles90.00, 92.63, 90.00
Refinement procedure
Resolution29.670 - 2.190
R-factor0.1611
Rwork0.159
R-free0.19250
Structure solution methodMOLECULAR REPLACEMENT
RMSD bond length0.004
RMSD bond angle0.546
Data reduction softwareXDS
Data scaling softwareAimless
Phasing softwarePHASER
Refinement softwarePHENIX ((1.20.1_4487: ???))
Data quality characteristics
 OverallOuter shell
Low resolution limit [Å]29.6702.260
High resolution limit [Å]2.1902.190
Rmerge0.0760.464
Rmeas0.538
Rpim0.268
Number of reflections268632185
<I/σ(I)>10.43.3
Completeness [%]99.5
Redundancy3.8
CC(1/2)0.9970.866
Crystallization Conditions
crystal IDmethodpHtemperaturedetails
1VAPOR DIFFUSION, HANGING DROP8.52930.12M Alcohol mix (0.2M 1,6-Hexanediol; 0.2M 1-Butanol; 0.2M 1,2-Propanediol; 0.2M 2-Propanol; 0.2M 1,4-Butanediol; 0.2M 1,3-Propanediol), 1.0M Tris (base); BICINE,60% Precipitant Mix (40% v/v PEG 500* MME; 20 % w/v PEG 20000)

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