5VF3

Bacteriophage T4 isometric capsid


ELECTRON MICROSCOPY
Sample
Enterobacteria phage T4
Specimen Preparation
Sample Aggregation State2D ARRAY
Vitrification InstrumentGATAN CRYOPLUNGE 3
Cryogen NameETHANE
Sample Vitrification DetailsBlot for 8 seconds before plunging.
3D Reconstruction
Reconstruction MethodSINGLE PARTICLE
Number of Particles18000
Reported Resolution (Å)3.3
Resolution MethodFSC 0.143 CUT-OFF
Other DetailsIndependent refinement of even/odd map, gold standard
Refinement Type
Symmetry TypePOINT
Point SymmetryI
Map-Model Fitting and Refinement
Id1
Refinement SpaceREAL
Refinement ProtocolAB INITIO MODEL
Refinement Target
Overall B Value
Fitting Procedure
Details
Data Acquisition
Detector TypeGATAN K2 SUMMIT (4k x 4k)
Electron Dose (electrons/Å**2)26
Imaging Experiment1
Date of Experiment
Temperature (Kelvin)
Microscope ModelFEI TITAN KRIOS
Minimum Defocus (nm)-1000
Maximum Defocus (nm)-3000
Minimum Tilt Angle (degrees)
Maximum Tilt Angle (degrees)
Nominal CS2.7
Imaging ModeBRIGHT FIELD
Specimen Holder ModelOTHER
Nominal Magnification18000
Calibrated Magnification18000
SourceFIELD EMISSION GUN
Acceleration Voltage (kV)300
Imaging DetailsData collection by Leginon
EM Software
TaskSoftware PackageVersion
MODEL FITTINGCoot
MODEL REFINEMENTPHENIX
FINAL EULER ASSIGNMENTEMAN, JSPR
CLASSIFICATIONRELION
Image Processing
CTF Correction TypeCTF Correction DetailsNumber of Particles SelectedParticle Selection Details
PHASE FLIPPING ONLYCTF amplitude correction was performed during 3D reconstruction.19000Approximately 1000 manually-picked particles were used for 2D classification. Templates were then generated from these 2D classes and used for automated particle picking.