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EMD-1042
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Title:
ATP-bound states of GroEL captured by cryo-electron microscopy.
Authors:
H.R. Saibil
Sample:
GroEL chaperonin, unliganded
Aggregation state:
Single particle (10.3 angstroms resolution)
Latest update:
2011-05-26
Summary
Experimental details
Visualization
Map information
Downloads
Sample
Sample name:
GroEL chaperonin, unliganded
Oligomeric state:
14-mer
Theoretical molecular weight of the sample:
0.8
Components:
ID
Type
Name
Exp. MW (MDa)
Oligomeric details
Recombinant expression
Synthetic
Organism
GO identifier
InterPro identifier
Virus identifier
Details
1
protein
GroEL
0.8
14-mer
true
Escherichia coli
Experiment
Sample preparation:
pH
Sample conc.
Details
Staining
Sample support details
7.5
0.8 mg/mL
12.5 mM HEPES, 5 mM KCl, 5 mM MgCl2
holey carbon film
Vitrification:
Cryogen name
Humidity
Temp.
Instr.
Method
Time resolved
Details
ETHANE
%
100 K
HOMEMADE PLUNGER
Blot for 1 second before plunging
ms
Vitrification instrument: self-made
Imaging:
Microscope
Voltage
Illumination mode
Imaging mode
Cs:
Defocus min.
Defocus max.
Nominal mag.
Calibrated mag.
Electron source
Detector
Detector distance
Astigmatism
FEI/PHILIPS CM200FEG/ST
200 kV
FLOOD BEAM
BRIGHT FIELD
2 mm
800 nm
1900 nm
38000
40220
FIELD EMISSION GUN
Kodak SO163 film
mm
Specimen holder
Holder model
Tilt min.
Tilt max.
Energy filter
Energy window
Temp.
Temp. min.
Temp. max.
Beam tilt
Electron dose
Other details
Date
Eucentric
GATAN LIQUID NITROGEN
°
°
eV
105 K
K
K
mrad
20 e/Å
2
Processing
Software:
Spider
CTF correction:
CTF multiplication and merging of 2D averages
Resolution by author:
10.3 Å
Resolution method:
FSC at 0.5
Processing details:
Filtered back projection
Unit cell:
Scanned images:
Num. images
Sampling size
OD range
Quant. bit number
Other details
Scanner
50
7 μm/pixel
1
8
link
ZEISS SCAI
Fitting:
PDB
Protocol
Target crit.
Software
B value
Fitting space
PDB chain
Details
1DER
Rigid body
DockEM
REAL
Manual fitting of the 3 domains of a subunit as rigid bodies using O, followed by refinement with DockEM
1GR5
pdb entry of the same structure