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- EMDB-9896: CryoEM structure of S.typhimurium R-type flagellar filament made ... -
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Open data
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Basic information
Entry | Database: EMDB / ID: EMD-9896 | |||||||||
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Title | CryoEM structure of S.typhimurium R-type flagellar filament made of FljB (A461V) without domain D3 by masking out | |||||||||
![]() | CryoEM structure of S.typhimurium R-type straight flagellar filament made of FljB (A461V) | |||||||||
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![]() | FljB / Helical reconstruction / Salmonella / Flagellar motor / PROTEIN FIBRIL | |||||||||
Function / homology | ![]() bacterial-type flagellum filament / bacterial-type flagellum-dependent cell motility / structural molecule activity / extracellular region Similarity search - Function | |||||||||
Biological species | ![]() | |||||||||
Method | helical reconstruction / cryo EM / Resolution: 3.56 Å | |||||||||
![]() | Yamaguchi T / Toma S | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Structural and Functional Comparison of Flagellar Filaments Composed of FljB and FliC. Authors: Tomoko Yamaguchi / Shoko Toma / Naoya Terahara / Tomoko Miyata / Masamichi Ashihara / Tohru Minamino / Keiichi Namba / Takayuki Kato / ![]() Abstract: The bacterial flagellum is a motility organelle consisting of a long helical filament as a propeller and a rotary motor that drives rapid filament rotation to produce thrust. serovar Typhimurium has ...The bacterial flagellum is a motility organelle consisting of a long helical filament as a propeller and a rotary motor that drives rapid filament rotation to produce thrust. serovar Typhimurium has two genes of flagellin, and , for flagellar filament formation and autonomously switches their expression at a frequency of 10-10 per cell per generation. We report here differences in their structures and motility functions under high-viscosity conditions. A strain expressing FljB showed a higher motility than one expressing FliC under high viscosity. To examine the reasons for this motility difference, we carried out structural analyses of the FljB filament by electron cryomicroscopy and found that the structure was nearly identical to that of the FliC filament except for the position and orientation of the outermost domain D3 of flagellin. The density of domain D3 was much lower in FljB than FliC, suggesting that domain D3 of FljB is more flexible and mobile than that of FliC. These differences suggest that domain D3 plays an important role not only in changing antigenicity of the filament but also in optimizing motility function of the filament as a propeller under different conditions. | |||||||||
History |
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Structure visualization
Movie |
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Structure viewer | EM map: ![]() ![]() ![]() |
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 228.9 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 17.9 KB 17.9 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 14.2 KB | Display | ![]() |
Images | ![]() | 2 MB | ||
Masks | ![]() | 244.1 MB | ![]() | |
Filedesc metadata | ![]() | 6.1 KB | ||
Others | ![]() ![]() | 194.5 MB 194.5 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 6jy0MC ![]() 0980C C: citing same article ( M: atomic model generated by this map |
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Similar structure data |
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Links
EMDB pages | ![]() ![]() |
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Map
File | ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | CryoEM structure of S.typhimurium R-type straight flagellar filament made of FljB (A461V) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.06 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Mask #1
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Projections & Slices |
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Density Histograms |
-Half map: EM half map-1 of 3D Refinement CryoEM structure...
File | emd_9896_half_map_1.map | ||||||||||||
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Annotation | EM half map-1 of 3D Refinement CryoEM structure of S.typhimurium R-type straight flagellar filament made of FljB (A461V) | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: EM half map-2 of 3D Refinement CryoEM structure...
File | emd_9896_half_map_2.map | ||||||||||||
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Annotation | EM half map-2 of 3D Refinement CryoEM structure of S.typhimurium R-type straight flagellar filament made of FljB (A461V) | ||||||||||||
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Density Histograms |
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Sample components
-Entire : FljB
Entire | Name: FljB |
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Components |
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-Supramolecule #1: FljB
Supramolecule | Name: FljB / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all / Details: R-type straight flagellar filament (A461V) |
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Source (natural) | Organism: ![]() Strain: SJW590 |
-Macromolecule #1: Flagellin
Macromolecule | Name: Flagellin / type: protein_or_peptide / ID: 1 / Number of copies: 22 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Molecular weight | Theoretical: 52.608449 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MAQVINTNSL SLLTQNNLNK SQSALGTAIE RLSSGLRINS AKDDAAGQAI ANRFTANIKG LTQASRNAND GISIAQTTEG ALNEINNNL QRVRELAVQS ANSTNSQSDL DSIQAEITQR LNEIDRVSGQ TQFNGVKVLA QDNTLTIQVG ANDGETIDID L KQINSQTL ...String: MAQVINTNSL SLLTQNNLNK SQSALGTAIE RLSSGLRINS AKDDAAGQAI ANRFTANIKG LTQASRNAND GISIAQTTEG ALNEINNNL QRVRELAVQS ANSTNSQSDL DSIQAEITQR LNEIDRVSGQ TQFNGVKVLA QDNTLTIQVG ANDGETIDID L KQINSQTL GLDSLNVQKA YDVKDTAVTT KAYANNGTTL DVSGLDDAAI KAATGGTNGT ASVTGGAVKF DADNNKYFVT IG GFTGADA AKNGDYEVNV ATDGTVTLAA GATKTTMPAG ATTKTEVQEL KDTPAVVSAD AKNALIAGGV DATDANGAEL VKM SYTDKN GKTIEGGYAL KAGDKYYAAD YDEATGAIKA KTTSYTAADG TTKTAANQLG GVDGKTEVVT IDGKTYNASK AAGH DFKAQ PELAEAAAKT TENPLQKIDA ALAQVDALRS DLGAVQNRFN SAITNLGNTV NNLSEVRSRI EDSDYATEVS NMSRA QILQ QAGTSVLAQA NQVPQNVLSL LR UniProtKB: Flagellin |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | helical reconstruction |
Aggregation state | filament |
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Sample preparation
Buffer | pH: 7.8 Component:
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Sugar embedding | Material: buffer | ||||||||||||
Grid | Model: Quantifoil, UltrAuFoil, R1.2/1.3 / Material: MOLYBDENUM / Support film - topology: CONTINUOUS / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 24 sec. / Pretreatment - Atmosphere: AIR | ||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: FEI FALCON II (4k x 4k) / Detector mode: COUNTING / Digitization - Frames/image: 1-6 / Number grids imaged: 3 / Number real images: 2319 / Average electron dose: 10.3 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | C2 aperture diameter: 100.0 µm / Calibrated defocus max: 1.6 µm / Calibrated defocus min: 0.21 µm / Calibrated magnification: 72273 / Illumination mode: OTHER / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.5 µm / Nominal magnification: 75000 |
Sample stage | Cooling holder cryogen: NITROGEN |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |