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Yorodumi- EMDB-17775: Subtomogram average of the Campylobacter jejuni flgPQ deletion fl... -
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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | Subtomogram average of the Campylobacter jejuni flgPQ deletion flagellar motor | |||||||||
Map data | Subtomogram average of the Campylobacter jejuni flgPQ deletion mutant flagellar motor | |||||||||
Sample |
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Keywords | flagellum / motor / Campylobacter jejuni / basal disk / MOTOR PROTEIN | |||||||||
| Biological species | ![]() | |||||||||
| Method | subtomogram averaging / cryo EM / Resolution: 36.2 Å | |||||||||
Authors | Cohen EJ / Beeby M | |||||||||
| Funding support | United Kingdom, 1 items
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Citation | Journal: Dev Cell / Year: 2024Title: Evolution of a large periplasmic disk in Campylobacterota flagella enables both efficient motility and autoagglutination. Authors: Eli J Cohen / Tina Drobnič / Deborah A Ribardo / Aoba Yoshioka / Trishant Umrekar / Xuefei Guo / Jose-Jesus Fernandez / Emma E Brock / Laurence Wilson / Daisuke Nakane / David R Hendrixson / Morgan Beeby / ![]() Abstract: The flagellar motors of Campylobacter jejuni (C. jejuni) and related Campylobacterota (previously epsilonproteobacteria) feature 100-nm-wide periplasmic "basal disks" that have been implicated in ...The flagellar motors of Campylobacter jejuni (C. jejuni) and related Campylobacterota (previously epsilonproteobacteria) feature 100-nm-wide periplasmic "basal disks" that have been implicated in scaffolding a wider ring of additional motor proteins to increase torque, but the size of these disks is excessive for a role solely in scaffolding motor proteins. Here, we show that the basal disk is a flange that braces the flagellar motor during disentanglement of its flagellar filament from interactions with the cell body and other filaments. We show that motor output is unaffected when we shrink or displace the basal disk, and suppressor mutations of debilitated motors occur in flagellar-filament or cell-surface glycosylation pathways, thus sidestepping the need for a flange to overcome the interactions between two flagellar filaments and between flagellar filaments and the cell body. Our results identify unanticipated co-dependencies in the evolution of flagellar motor structure and cell-surface properties in the Campylobacterota. | |||||||||
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_17775.map.gz | 36.7 MB | EMDB map data format | |
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| Header (meta data) | emd-17775-v30.xml emd-17775.xml | 13.1 KB 13.1 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_17775_fsc.xml | 10.1 KB | Display | FSC data file |
| Images | emd_17775.png | 37.8 KB | ||
| Filedesc metadata | emd-17775.cif.gz | 4.2 KB | ||
| Others | emd_17775_half_map_1.map.gz emd_17775_half_map_2.map.gz | 37.4 MB 37.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-17775 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-17775 | HTTPS FTP |
-Related structure data
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Map
| File | Download / File: emd_17775.map.gz / Format: CCP4 / Size: 40.6 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Subtomogram average of the Campylobacter jejuni flgPQ deletion mutant flagellar motor | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 7.6 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: #1
| File | emd_17775_half_map_1.map | ||||||||||||
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| Density Histograms |
-Half map: #2
| File | emd_17775_half_map_2.map | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Campylobacter jejuni flagellar motor
| Entire | Name: Campylobacter jejuni flagellar motor |
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| Components |
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-Supramolecule #1: Campylobacter jejuni flagellar motor
| Supramolecule | Name: Campylobacter jejuni flagellar motor / type: organelle_or_cellular_component / ID: 1 / Parent: 0 |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | subtomogram averaging |
| Aggregation state | cell |
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Sample preparation
| Buffer | pH: 7.2 |
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| Grid | Model: Quantifoil R2/2 / Material: COPPER / Mesh: 200 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 60 sec. |
| Vitrification | Cryogen name: ETHANE / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS GLACIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 4.0 e/Å2 |
| Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | C2 aperture diameter: 50.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.0 µm / Nominal defocus min: 3.0 µm |
| Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
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Keywords
Authors
United Kingdom, 1 items
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Processing
FIELD EMISSION GUN
