+ Open data
Open data
- Basic information
Basic information
| Entry | Database: EMDB / ID: EMD-1949 | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Title | Human dynamin 1 deltaPRD polymer stabilized with GMPPCP | |||||||||
|  Map data | Three-dimensional volume of deltaPRD human dynamin 1 polymer | |||||||||
|  Sample | 
 | |||||||||
|  Keywords | dynamin / endocytosis / GTP hydrolysis / membrane remodeling | |||||||||
| Function / homology |  Function and homology information clathrin coat assembly involved in endocytosis / vesicle scission / synaptic vesicle budding from presynaptic endocytic zone membrane / interleukin-27-mediated signaling pathway / dynamin GTPase / chromaffin granule / regulation of vesicle size / Retrograde neurotrophin signalling / Toll Like Receptor 4 (TLR4) Cascade / Formation of annular gap junctions ...clathrin coat assembly involved in endocytosis / vesicle scission / synaptic vesicle budding from presynaptic endocytic zone membrane / interleukin-27-mediated signaling pathway / dynamin GTPase / chromaffin granule / regulation of vesicle size / Retrograde neurotrophin signalling / Toll Like Receptor 4 (TLR4) Cascade / Formation of annular gap junctions / endosome organization / Gap junction degradation / response to type I interferon / negative regulation of viral genome replication / phosphatidylinositol-3,4,5-trisphosphate binding / Recycling pathway of L1 / EPH-ephrin mediated repulsion of cells / endocytic vesicle / clathrin-coated pit / phosphatidylinositol-4,5-bisphosphate binding / antiviral innate immune response / MHC class II antigen presentation / receptor-mediated endocytosis / cell projection / defense response / protein homooligomerization / receptor internalization / ISG15 antiviral mechanism / response to virus / endocytosis / Interferon alpha/beta signaling / GDP binding / presynapse / Clathrin-mediated endocytosis / nuclear membrane / protein homotetramerization / microtubule binding / defense response to virus / microtubule / innate immune response / GTPase activity / apoptotic process / synapse / endoplasmic reticulum membrane / protein kinase binding / GTP binding / perinuclear region of cytoplasm / signal transduction / protein homodimerization activity / RNA binding / extracellular exosome / identical protein binding / nucleus / plasma membrane / cytoplasm / cytosol Similarity search - Function | |||||||||
| Biological species |  Homo sapiens (human) | |||||||||
| Method | helical reconstruction / cryo EM / Resolution: 12.2 Å | |||||||||
|  Authors | Chappie JS / Mears JA / Fang S / Leonard M / Schmid SL / Milligan RA / Hinshaw JE / Dyda F | |||||||||
|  Citation |  Journal: Cell / Year: 2011 Title: A pseudoatomic model of the dynamin polymer identifies a hydrolysis-dependent powerstroke. Authors: Joshua S Chappie / Jason A Mears / Shunming Fang / Marilyn Leonard / Sandra L Schmid / Ronald A Milligan / Jenny E Hinshaw / Fred Dyda /  Abstract: The GTPase dynamin catalyzes membrane fission by forming a collar around the necks of clathrin-coated pits, but the specific structural interactions and conformational changes that drive this process ...The GTPase dynamin catalyzes membrane fission by forming a collar around the necks of clathrin-coated pits, but the specific structural interactions and conformational changes that drive this process remain a mystery. We present the GMPPCP-bound structures of the truncated human dynamin 1 helical polymer at 12.2 Å and a fusion protein, GG, linking human dynamin 1's catalytic G domain to its GTPase effector domain (GED) at 2.2 Å. The structures reveal the position and connectivity of dynamin fragments in the assembled structure, showing that G domain dimers only form between tetramers in sequential rungs of the dynamin helix. Using chemical crosslinking, we demonstrate that dynamin tetramers are made of two dimers, in which the G domain of one molecule interacts in trans with the GED of another. Structural comparison of GG(GMPPCP) to the GG transition-state complex identifies a hydrolysis-dependent powerstroke that may play a role in membrane-remodeling events necessary for fission. | |||||||||
| History | 
 | 
- Structure visualization
Structure visualization
| Movie | 
 
 
  Movie viewer | 
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| Structure viewer | EM map:  SurfView  Molmil  Jmol/JSmol | 
| Supplemental images | 
- Downloads & links
Downloads & links
-EMDB archive
| Map data |  emd_1949.map.gz | 7.2 MB |  EMDB map data format | |
|---|---|---|---|---|
| Header (meta data) |  emd-1949-v30.xml  emd-1949.xml | 14.8 KB 14.8 KB | Display Display |  EMDB header | 
| Images |  emd_1949.tif | 360.3 KB | ||
| Archive directory |  http://ftp.pdbj.org/pub/emdb/structures/EMD-1949  ftp://ftp.pdbj.org/pub/emdb/structures/EMD-1949 | HTTPS FTP | 
-Validation report
| Summary document |  emd_1949_validation.pdf.gz | 283 KB | Display |  EMDB validaton report | 
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| Full document |  emd_1949_full_validation.pdf.gz | 282.1 KB | Display | |
| Data in XML |  emd_1949_validation.xml.gz | 6.4 KB | Display | |
| Arichive directory |  https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1949  ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-1949 | HTTPS FTP | 
-Related structure data
| Related structure data |  3zysMC  3zycC M: atomic model generated by this map C: citing same article ( | 
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| Similar structure data | 
- Links
Links
| EMDB pages |  EMDB (EBI/PDBe) /  EMDataResource | 
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| Related items in Molecule of the Month | 
- Map
Map
| File |  Download / File: emd_1949.map.gz / Format: CCP4 / Size: 29.8 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Annotation | Three-dimensional volume of deltaPRD human dynamin 1 polymer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
 
 Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 2.26 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Density | 
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Details | EMDB XML: 
 CCP4 map header: 
 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
-Supplemental data
- Sample components
Sample components
-Entire : GMPPCP-stablized human dynamin 1 delta PRD polymer
| Entire | Name: GMPPCP-stablized human dynamin 1 delta PRD polymer | 
|---|---|
| Components | 
 | 
-Supramolecule #1000: GMPPCP-stablized human dynamin 1 delta PRD polymer
| Supramolecule | Name: GMPPCP-stablized human dynamin 1 delta PRD polymer / type: sample / ID: 1000 / Oligomeric state: Helical assembly of dynamin tetramers / Number unique components: 3 | 
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-Macromolecule #1: Human dynamin 1 delta PRD
| Macromolecule | Name: Human dynamin 1 delta PRD / type: protein_or_peptide / ID: 1 / Name.synonym: Human dynamin 1 delta PRD / Details: contains bound GMPPCP / Oligomeric state: Dimer / Recombinant expression: Yes | 
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| Source (natural) | Organism:  Homo sapiens (human) / synonym: Human / Location in cell: Plasma membrane and cytosol | 
| Recombinant expression | Organism:   Escherichia coli BL21(DE3) (bacteria) / Recombinant plasmid: PMALC2XP5D | 
-Macromolecule #2: Human dynamin 1 pleckstrin homology domain
| Macromolecule | Name: Human dynamin 1 pleckstrin homology domain / type: protein_or_peptide / ID: 2 / Name.synonym: Human dynamin 1 pleckstrin homology domain / Oligomeric state: Dimer / Recombinant expression: Yes | 
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| Source (natural) | Organism:  Homo sapiens (human) / synonym: Human / Location in cell: Plasma membrane and cytosol | 
| Recombinant expression | Organism:   Escherichia coli BL21(DE3) (bacteria) / Recombinant plasmid: PSKB-LNB | 
-Macromolecule #3: Interferon-induced GTP-binding protein Mx1
| Macromolecule | Name: Interferon-induced GTP-binding protein Mx1 / type: protein_or_peptide / ID: 3 / Name.synonym: Interferon-induced GTP-binding protein Mx1 / Oligomeric state: Dimer / Recombinant expression: Yes | 
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| Source (natural) | Organism:  Homo sapiens (human) / synonym: Human | 
| Recombinant expression | Organism:   Escherichia coli (E. coli) / Recombinant plasmid: PET11A | 
-Experimental details
-Structure determination
| Method | cryo EM | 
|---|---|
|  Processing | helical reconstruction | 
| Aggregation state | filament | 
- Sample preparation
Sample preparation
| Concentration | 0.5 mg/mL | 
|---|---|
| Buffer | pH: 7.5 Details: 20 mM Hepes pH 7.5, 50 mM NaCl, 2 mM EGTA, 4 mM MgCl2, 1 mM DTT, 1 mg/ml 0.4 um 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS) liposomes, 2 mM GMPPCP | 
| Grid | Details: 400 mesh C-flat grids | 
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 93 K / Instrument: HOMEMADE PLUNGER / Details: Vitrification instrument: Manual Method: Absorbed samples to grids, blotted, washed with 20 mM Hepes pH 7.5, blotted and plunged. | 
- Electron microscopy
Electron microscopy
| Microscope | FEI TECNAI 20 | 
|---|---|
| Temperature | Min: 93 K / Max: 95 K | 
| Alignment procedure | Legacy - Astigmatism: objective lens astigmatism was corrected at 100,000X magnification | 
| Image recording | Category: CCD / Film or detector model: GATAN ULTRASCAN 4000 (4k x 4k) / Average electron dose: 10 e/Å2 / Details: Images were collected on CCD | 
| Tilt angle min | 0 | 
| Tilt angle max | 0 | 
| Electron beam | Acceleration voltage: 120 kV / Electron source:  FIELD EMISSION GUN | 
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2 mm / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.5 µm / Nominal magnification: 50000 | 
| Sample stage | Specimen holder: Gatan 626 side entry cryo-stage / Specimen holder model: GATAN LIQUID NITROGEN | 
- Image processing
Image processing
| Final reconstruction | Applied symmetry - Helical parameters - Δz: 7.52 Å Applied symmetry - Helical parameters - Δ&Phi: 27.3 ° Algorithm: OTHER / Resolution.type: BY AUTHOR / Resolution: 12.2 Å / Resolution method: FSC 0.5 CUT-OFF / Software - Name: Spider Details: A total of 4,814 helical segments were incorporated by the IHRSR algorithm into the final reconstruction after 50 cycles | 
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| CTF correction | Details: Each image using ACE2 | 
-Atomic model buiding 1
| Initial model | PDB ID: Chain - Chain ID: A | 
|---|---|
| Software | Name: YUP | 
| Details | PDBEntryID_givenInChain. Protocol: Manual and Flexible fitting. Models were initially placed manually and initial positions were refined using the YUP.SCX method of the YUP software package | 
| Refinement | Space: REAL / Protocol: FLEXIBLE FIT | 
| Output model |  PDB-3zys:  | 
-Atomic model buiding 2
| Initial model | PDB ID: Chain - Chain ID: A | 
|---|---|
| Software | Name: YUP | 
| Details | PDBEntryID_givenInChain. Protocol: Manual and Flexible fitting. Models were initially placed manually and initial positions were refined using the YUP.SCX method of the YUP software package | 
| Refinement | Space: REAL / Protocol: FLEXIBLE FIT | 
| Output model |  PDB-3zys:  | 
-Atomic model buiding 3
| Initial model | PDB ID: Chain - Chain ID: A | 
|---|---|
| Software | Name: YUP | 
| Details | PDBEntryID_givenInChain. Protocol: Manual and Flexible fitting. Models were initially placed manually and initial positions were refined using the YUP.SCX method of the YUP software package | 
| Refinement | Space: REAL / Protocol: FLEXIBLE FIT | 
| Output model |  PDB-3zys:  | 
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