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- EMDB-41263: Purified alpha-CaMKII Holoenzymes -

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Basic information

Entry
Database: EMDB / ID: EMD-41263
TitlePurified alpha-CaMKII Holoenzymes
Map data
Sample
  • Complex: Purified alpha-CaMKII Holoenzyme
KeywordsCaMKII / calmodulin / tomography / segmentation / SIGNALING PROTEIN
Biological speciesRattus norvegicus (Norway rat)
Methodelectron tomography / cryo EM
AuthorsSwulius MT
Funding support United States, 1 items
OrganizationGrant numberCountry
National Institutes of Health/National Institute of Neurological Disorders and Stroke (NIH/NINDS) United States
CitationJournal: To be Published
Title: Rapid Synthesis of Cryo-ET Data for Training Deep Learning Models.
Authors: Purnell C / Heebner J / Hylton RH / Kabonick S / Grillo M / Grigoryev S / Heberle F / Waxham NM / Swulius MT
History
DepositionJul 16, 2023-
Header (metadata) releaseJul 17, 2024-
Map releaseJul 17, 2024-
UpdateJul 17, 2024-
Current statusJul 17, 2024Processing site: RCSB / Status: Released

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Structure visualization

Supplemental images

Downloads & links

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Map

FileDownload / File: emd_41263.map.gz / Format: CCP4 / Size: 120.8 MB / Type: IMAGE STORED AS SIGNED BYTE
Voxel sizeX=Y=Z: 5.4 Å
Density
Minimum - Maximum-128.0 - 127.0
Average (Standard dev.)-0.9256713 (±25.199891999999998)
SymmetrySpace group: 1
Details

EMDB XML:

Map geometry
Axis orderXYZ
Origin000
Dimensions1440102386
Spacing1023144086
CellA: 5524.2 Å / B: 7776.0 Å / C: 464.4 Å
α=β=γ: 90.0 °

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Supplemental data

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Additional map: #1

Fileemd_41263_additional_1.map
Projections & Slices
AxesZYX

Projections

Slices (1/2)
Density Histograms

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Sample components

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Entire : Purified alpha-CaMKII Holoenzyme

EntireName: Purified alpha-CaMKII Holoenzyme
Components
  • Complex: Purified alpha-CaMKII Holoenzyme

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Supramolecule #1: Purified alpha-CaMKII Holoenzyme

SupramoleculeName: Purified alpha-CaMKII Holoenzyme / type: complex / ID: 1 / Parent: 0
Details: Weighted Back-projection and Greyscale Segmentation
Source (natural)Organism: Rattus norvegicus (Norway rat)

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Experimental details

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Structure determination

Methodcryo EM
Processingelectron tomography
Aggregation stateparticle

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Sample preparation

BufferpH: 6.8
VitrificationCryogen name: ETHANE
SectioningOther: NO SECTIONING

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Electron microscopy

MicroscopeTFS KRIOS
Image recordingFilm or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 1.0 e/Å2
Electron beamAcceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN
Electron opticsIllumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 5.0 µm / Nominal defocus min: 5.0 µm
Experimental equipment
Model: Titan Krios / Image courtesy: FEI Company

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Image processing

Final reconstructionNumber images used: 60

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