6SP2

CryoEM structure of SERINC from Drosophila melanogaster


ELECTRON MICROSCOPY
Sample
SERINC homo-hexamer
Specimen Preparation
Sample Aggregation StatePARTICLE
Vitrification InstrumentFEI VITROBOT MARK IV
Cryogen NameETHANE
Sample Vitrification Detailswait 60 seconds, blot for 3-4 seconds
3D Reconstruction
Reconstruction MethodSINGLE PARTICLE
Number of Particles159252
Reported Resolution (Å)3.33
Resolution MethodFSC 0.143 CUT-OFF
Other Details
Refinement Type
Symmetry TypePOINT
Point SymmetryC6
Map-Model Fitting and Refinement
Id1
Refinement SpaceREAL
Refinement ProtocolAB INITIO MODEL
Refinement TargetCross-correlation coefficient
Overall B Value150.6
Fitting Procedure
Details
Data Acquisition
Detector TypeGATAN K2 QUANTUM (4k x 4k)
Electron Dose (electrons/Å**2)50
Imaging Experiment1
Date of Experiment
Temperature (Kelvin)
Microscope ModelFEI TITAN KRIOS
Minimum Defocus (nm)
Maximum Defocus (nm)
Minimum Tilt Angle (degrees)
Maximum Tilt Angle (degrees)
Nominal CS
Imaging ModeBRIGHT FIELD
Specimen Holder Model
Nominal Magnification
Calibrated Magnification
SourceFIELD EMISSION GUN
Acceleration Voltage (kV)300
Imaging Details
EM Software
TaskSoftware PackageVersion
PARTICLE SELECTIONRELION2.1
MODEL FITTINGCoot
INITIAL EULER ASSIGNMENTcryoSPARC2
FINAL EULER ASSIGNMENTcryoSPARC2
CLASSIFICATIONRELION2.1
RECONSTRUCTIONcryoSPARC2
MODEL REFINEMENTPHENIX
Image Processing
CTF Correction TypeCTF Correction DetailsNumber of Particles SelectedParticle Selection Details
NONE1857080A sub-set of particles semi-automatically picked in EMAN2 Boxer were used to generate the starting 2D class averages, which, upon low-pass filtering to 20 A, served as templates for auto-picking of the entire dataset.