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Yorodumi- EMDB-60565: Flagellar central pair apparatus of Chlamydomonas reinhardtii FAP... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-60565 | |||||||||
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Title | Flagellar central pair apparatus of Chlamydomonas reinhardtii FAP47-deficient mutant. | |||||||||
Map data | Flagellar central pair apparatus of Chlamydomonas reinhardtii FAP47-deficient mutant. | |||||||||
Sample |
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Keywords | cilia/flagella / Chlamydomonas / MOTOR PROTEIN | |||||||||
Biological species | Chlamydomonas reinhardtii (plant) | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 45.3 Å | |||||||||
Authors | Tani Y / Yanagisawa H / Kikkawa M | |||||||||
Funding support | Japan, 2 items
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Citation | Journal: Cytoskeleton (Hoboken) / Year: 2024 Title: Structure and function of FAP47 in the central pair apparatus of Chlamydomonas flagella. Authors: Yuma Tani / Haruaki Yanagisawa / Toshiki Yagi / Masahide Kikkawa / Abstract: Motile cilia have a so-called "9 + 2" structure, which consists of nine doublet microtubules and a central pair apparatus. The central pair apparatus (CA) is thought to interact mechanically with ...Motile cilia have a so-called "9 + 2" structure, which consists of nine doublet microtubules and a central pair apparatus. The central pair apparatus (CA) is thought to interact mechanically with radial spokes and to control the flagellar beating. Recently, the components of the CA have been identified by proteomic and genomic analyses. Still, the mechanism of how the CA contributes to ciliary motility has much to be revealed. Here, we focused on one CA component with a large molecular weight: FAP47, and its relationship with two other CA components with large molecular weight: HYDIN, and CPC1. The analyses of motility of the Chlamydomonas mutants revealed that in contrast to cpc1 or hydin, which swam more slowly than the wild type, fap47 cells displayed wild-type swimming velocity and flagellar beat frequency, yet interestingly, fap47 cells have phototaxis defects and swim straighter than the wild-type cells. Furthermore, the double mutant fap47cpc1 and fap47hydin showed significantly slower swimming than cpc1 and hydin cells, and the motility defect of fap47cpc1 was rescued to the cpc1 level with GFP-tagged FAP47, indicating that the lack of FAP47 makes the motility defect of cpc1 worse. Cryo-electron tomography demonstrated that the fap47 lacks a part of the C1-C2 bridge of CA. Taken together, these observations indicate that FAP47 maintains the structural stiffness of the CA, which is important for flagellar regulation. | |||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_60565.map.gz | 9.9 MB | EMDB map data format | |
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Header (meta data) | emd-60565-v30.xml emd-60565.xml | 11.8 KB 11.8 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_60565_fsc.xml | 9.3 KB | Display | FSC data file |
Images | emd_60565.png | 74.2 KB | ||
Filedesc metadata | emd-60565.cif.gz | 3.8 KB | ||
Others | emd_60565_half_map_1.map.gz emd_60565_half_map_2.map.gz | 28.4 MB 28.4 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-60565 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-60565 | HTTPS FTP |
-Validation report
Summary document | emd_60565_validation.pdf.gz | 851 KB | Display | EMDB validaton report |
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Full document | emd_60565_full_validation.pdf.gz | 850.6 KB | Display | |
Data in XML | emd_60565_validation.xml.gz | 13.6 KB | Display | |
Data in CIF | emd_60565_validation.cif.gz | 18.9 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-60565 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-60565 | HTTPS FTP |
-Related structure data
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_60565.map.gz / Format: CCP4 / Size: 30.5 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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Annotation | Flagellar central pair apparatus of Chlamydomonas reinhardtii FAP47-deficient mutant. | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 7.1 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #1
File | emd_60565_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #2
File | emd_60565_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Flagellar central pair apparatus of Chlamydomonas reinhardtii wil...
Entire | Name: Flagellar central pair apparatus of Chlamydomonas reinhardtii wild type |
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Components |
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-Supramolecule #1: Flagellar central pair apparatus of Chlamydomonas reinhardtii wil...
Supramolecule | Name: Flagellar central pair apparatus of Chlamydomonas reinhardtii wild type type: organelle_or_cellular_component / ID: 1 / Parent: 0 |
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Source (natural) | Organism: Chlamydomonas reinhardtii (plant) |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | subtomogram averaging |
Aggregation state | filament |
-Sample preparation
Buffer | pH: 7.3 |
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Vitrification | Cryogen name: ETHANE |
-Electron microscopy
Microscope | FEI TALOS ARCTICA |
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Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Average electron dose: 3.2 e/Å2 |
Electron beam | Acceleration voltage: 200 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 8.0 µm / Nominal defocus min: 6.0 µm |
Experimental equipment | Model: Talos Arctica / Image courtesy: FEI Company |