EMD-5410

Single-particle
6.5 Å
EMD-5410 Deposition: 07/04/2012
Map released: 30/01/2013
Last modified: 06/02/2013
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-5410

Cryo-electron microscopic reconstruction of wild rabbit hemorrhagic disease virus

EMD-5410

Single-particle
6.5 Å
EMD-5410 Deposition: 07/04/2012
Map released: 30/01/2013
Last modified: 06/02/2013
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Method: Single-particle
Aggregation State: Particle
Specimen preparation [1]
Buffer
pH: 7.0
Details: 50mM Tris, 50mM NaCl, 5mM EDTA
Grid
Details: 200 mesh copper grid with holey array carbon support (GiG), glow discharged
Vitrification
Cryogen name: ETHANE
Chamber humidity: 100%
Chamber temperature: 100 K
Instrument: FEI VITROBOT MARK IV
Method: Blot for 3 seconds before plunging
Microscopy [1]
Microscope: FEI TITAN KRIOS
Illumination mode: FLOOD BEAM
Imaging mode: BRIGHT FIELD
Electron source: FIELD EMISSION GUN
Acceleration voltage: 300 kV
Nominal CS: 2.7 mm
Nominal defocus: 1.5 µm - 2.5 µm
Nominal magnification: 96000.0
Calibrated magnification: 160770.0
Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER
Specimen holder details: Liquid nitrogen cooled
Alignment procedure: LEGACY (Astigmatism: Objective lens astigmatism was corrected at 100,000 times magnification, Electron beam tilt params: 0)
Minimum tilt angle: 0
Maximum tilt angle: 0
Temperature
Average: 85 K
Image Recording [1]
Detector category: CCD
Detector model: GATAN ULTRASCAN 4000 (4k x 4k)
Sampling interval: 15 µm
Number of real images: 1100
Average electron dose per image: 20 e/Å2
Bits per pixel: 32.0
Image processing [1]
Details: The particles were selected using an automatic selection program FindEM.
Final reconstruction
Resolution: 6.5 Å ( BY AUTHOR)
Resolution method: FSC 0.5 CUT-OFF
Number of images used: 26000
Algorithm: OTHER
Details: The final map was sharpened to 4.5 Angstrom with B factor -300 and then filtered to 5.0 Angstrom.
Applied Symmetry
Point group: I
Software [1]
Name Version Details
EMAN1.9, Spider - -
Final 2D classification
Number of classes: 475
CTF correction
Details:CTF correction of each whole micrograph
Map
Format: CCP4
Data type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)
Annotation details: Reconstruction of wild rabbit hemorrhagic disease virus; The final map was sharpened using b factor -300 A2 to 4.5 angstrom and low passed to 5 angstrom.
Details: ::::EMDATABANK.org::::EMD-5410::::
Geometry
X Y Z
Dimensions 480 480 480
Origin -240 -240 -240
Spacing 480 480 480
Voxel size 0.933 Å 0.933 Å 0.933 Å
Contour list
Primary Level Source
True 2.6 AUTHOR