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Yorodumi- EMDB-13527: Cryo-EM structure of the actomyosin-V complex in the strong-ADP s... -
+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-13527 | ||||||||||||||||||
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Title | Cryo-EM structure of the actomyosin-V complex in the strong-ADP state (central 1er, class 6) | ||||||||||||||||||
Map data | Sharpened map of the central actomyosin-V-LC molecule filtered to local resolution (class 6) | ||||||||||||||||||
Sample |
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Function / homology | Function and homology information minus-end directed microfilament motor activity / unconventional myosin complex / insulin-responsive compartment / vesicle transport along actin filament / muscle myosin complex / muscle filament sliding / myosin II complex / myosin complex / structural constituent of muscle / cytoskeletal motor activator activity ...minus-end directed microfilament motor activity / unconventional myosin complex / insulin-responsive compartment / vesicle transport along actin filament / muscle myosin complex / muscle filament sliding / myosin II complex / myosin complex / structural constituent of muscle / cytoskeletal motor activator activity / microfilament motor activity / tropomyosin binding / myosin heavy chain binding / mesenchyme migration / troponin I binding / filamentous actin / actin filament bundle / cytoskeletal motor activity / skeletal muscle thin filament assembly / actin filament bundle assembly / striated muscle thin filament / skeletal muscle myofibril / actin monomer binding / Smooth Muscle Contraction / skeletal muscle fiber development / stress fiber / vesicle-mediated transport / titin binding / skeletal muscle tissue development / muscle contraction / actin filament polymerization / filopodium / actin filament organization / protein localization to plasma membrane / actin filament / Hydrolases; Acting on acid anhydrides; Acting on acid anhydrides to facilitate cellular and subcellular movement / cellular response to insulin stimulus / calcium-dependent protein binding / actin filament binding / actin cytoskeleton / lamellipodium / cell body / vesicle / calmodulin binding / hydrolase activity / protein domain specific binding / Golgi membrane / calcium ion binding / positive regulation of gene expression / magnesium ion binding / extracellular exosome / ATP binding / identical protein binding / membrane / cytosol / cytoplasm Similarity search - Function | ||||||||||||||||||
Biological species | synthetic construct (others) / Homo sapiens (human) / Gallus gallus (chicken) / Oryctolagus cuniculus (rabbit) / Amanita phalloides (death cap) / Rabbit (rabbit) | ||||||||||||||||||
Method | helical reconstruction / cryo EM / Resolution: 3.6 Å | ||||||||||||||||||
Authors | Pospich S / Sweeney HL / Houdusse A / Raunser S | ||||||||||||||||||
Funding support | Germany, European Union, France, United States, 5 items
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Citation | Journal: Elife / Year: 2021 Title: High-resolution structures of the actomyosin-V complex in three nucleotide states provide insights into the force generation mechanism. Authors: Sabrina Pospich / H Lee Sweeney / Anne Houdusse / Stefan Raunser / Abstract: The molecular motor myosin undergoes a series of major structural transitions during its force-producing motor cycle. The underlying mechanism and its coupling to ATP hydrolysis and actin binding are ...The molecular motor myosin undergoes a series of major structural transitions during its force-producing motor cycle. The underlying mechanism and its coupling to ATP hydrolysis and actin binding are only partially understood, mostly due to sparse structural data on actin-bound states of myosin. Here, we report 26 high-resolution cryo-EM structures of the actomyosin-V complex in the strong-ADP, rigor, and a previously unseen post-rigor transition state that binds the ATP analog AppNHp. The structures reveal a high flexibility of myosin in each state and provide valuable insights into the structural transitions of myosin-V upon ADP release and binding of AppNHp, as well as the actomyosin interface. In addition, they show how myosin is able to specifically alter the structure of F-actin. | ||||||||||||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_13527.map.gz | 1.4 MB | EMDB map data format | |
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Header (meta data) | emd-13527-v30.xml emd-13527.xml | 28.7 KB 28.7 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_13527_fsc.xml | 11.7 KB | Display | FSC data file |
Images | emd_13527.png | 93.1 KB | ||
Masks | emd_13527_msk_1.map | 125 MB | Mask map | |
Others | emd_13527_additional_1.map.gz emd_13527_additional_2.map.gz emd_13527_half_map_1.map.gz emd_13527_half_map_2.map.gz | 1.5 MB 12.1 MB 59.6 MB 59.6 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-13527 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-13527 | HTTPS FTP |
-Validation report
Summary document | emd_13527_validation.pdf.gz | 413.4 KB | Display | EMDB validaton report |
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Full document | emd_13527_full_validation.pdf.gz | 412.9 KB | Display | |
Data in XML | emd_13527_validation.xml.gz | 18.6 KB | Display | |
Data in CIF | emd_13527_validation.cif.gz | 24 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-13527 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-13527 | HTTPS FTP |
-Related structure data
Related structure data | 7pmbMC 7pltC 7pluC 7plvC 7plwC 7plxC 7plyC 7plzC 7pm0C 7pm1C 7pm2C 7pm3C 7pm5C 7pm6C 7pm7C 7pm8C 7pm9C 7pmaC 7pmcC 7pmdC 7pmeC 7pmfC 7pmgC 7pmhC 7pmiC 7pmjC 7pmlC M: atomic model generated by this map C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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Related items in Molecule of the Month |
-Map
File | Download / File: emd_13527.map.gz / Format: CCP4 / Size: 125 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Annotation | Sharpened map of the central actomyosin-V-LC molecule filtered to local resolution (class 6) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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
File | emd_13527_msk_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Additional map: Sharpened map of the central actomyosin-V-LC molecule filtered...
File | emd_13527_additional_1.map | ||||||||||||
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Annotation | Sharpened map of the central actomyosin-V-LC molecule filtered to nominal resolution (class 6) | ||||||||||||
Projections & Slices |
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Density Histograms |
-Additional map: Denoised map of the central actomyosin-V-LC molecule (LAFTER,...
File | emd_13527_additional_2.map | ||||||||||||
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Annotation | Denoised map of the central actomyosin-V-LC molecule (LAFTER, class 6) | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half map (signal subtracted particles, class 6)
File | emd_13527_half_map_1.map | ||||||||||||
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Annotation | Half map (signal subtracted particles, class 6) | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Half map (signal subtracted particles, class 6)
File | emd_13527_half_map_2.map | ||||||||||||
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Annotation | Half map (signal subtracted particles, class 6) | ||||||||||||
Projections & Slices |
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Density Histograms |
-Sample components
+Entire : Actomyosin-V complex in the strong-ADP state
+Supramolecule #1: Actomyosin-V complex in the strong-ADP state
+Supramolecule #2: Phalloidin
+Supramolecule #3: Myosin light chain 6B
+Supramolecule #4: Unconventional myosin-Va
+Supramolecule #5: Actin, alpha skeletal muscle
+Macromolecule #1: Phalloidin
+Macromolecule #2: Myosin light chain 6B
+Macromolecule #3: Unconventional myosin-Va
+Macromolecule #4: Actin, alpha skeletal muscle
+Macromolecule #5: MAGNESIUM ION
+Macromolecule #6: ADENOSINE-5'-DIPHOSPHATE
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | helical reconstruction |
Aggregation state | filament |
-Sample preparation
Buffer | pH: 7.5 |
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Grid | Model: Quantifoil R2/1 / Material: COPPER / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Pretreatment - Type: GLOW DISCHARGE |
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 286 K / Instrument: FEI VITROBOT MARK III / Details: On grid decoration. |
Details | Rise 27.8 A, Twist -167.3 degrees |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: SUPER-RESOLUTION / Number grids imaged: 1 / Number real images: 5908 / Average exposure time: 15.0 sec. / Average electron dose: 82.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm |
Sample stage | Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER / Cooling holder cryogen: NITROGEN |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |