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Yorodumi- EMDB-72930: Plasmodium falciparum moving junction staple - Particle subtracte... -
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Open data
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Basic information
| Entry | ![]() | |||||||||
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| Title | Plasmodium falciparum moving junction staple - Particle subtracted, local refined C-terminus of PfRON5 | |||||||||
Map data | Local Refined C-terminus of PfRON5 | |||||||||
Sample |
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Keywords | Invasion / Plasmodium / Apicomplexa / CryoEM / Endogenous / MEMBRANE PROTEIN | |||||||||
| Biological species | ![]() | |||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 3.6 Å | |||||||||
Authors | Haile MT / Zhen J / Ho C | |||||||||
| Funding support | United States, 1 items
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Citation | Journal: Cell / Year: 2026Title: Structural basis for host membrane binding and remodeling by invading malaria parasites. Authors: Meseret T Haile / Daphne A Kaxiras / James Zhen / Carolyn L Lee / Britney Jiang / Jennifer L Small-Saunders / Chi-Min Ho / ![]() Abstract: The Plasmodium moving junction is central to malarial host-cell invasion, and yet its function remains unclear. Here, we determine the endogenous structure of the basic repeating unit of the moving ...The Plasmodium moving junction is central to malarial host-cell invasion, and yet its function remains unclear. Here, we determine the endogenous structure of the basic repeating unit of the moving junction, purified directly from invasion-stalled Plasmodium falciparum parasites, revealing a sailboat-shaped 1:1:1:1 assembly of apical membrane antigen 1 (PfAMA1) and rhoptry neck proteins 2, 4, and 5 (PfRON2, PfRON4, and PfRON5). We observe two PfRON2 transmembrane helices that anchor the complex in the red blood cell (RBC) membrane and display an extracellular handle for PfAMA1 binding. PfAMA1 directly contacts the RBC membrane, strengthening the connection. PfRON2/4/5 form a large, basic platform inside the RBC that electrostatically engages the RBC membrane and wedges seven amphipathic helices deep into the bilayer, suggesting an active role in host-membrane remodeling. We then leverage the native membrane context revealed by our structure, along with recent advances in computational protein design, to enable the rational design of a small protein binder that inhibits invasion. | |||||||||
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Structure visualization
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Downloads & links
-EMDB archive
| Map data | emd_72930.map.gz | 31.6 MB | EMDB map data format | |
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| Header (meta data) | emd-72930-v30.xml emd-72930.xml | 15.7 KB 15.7 KB | Display Display | EMDB header |
| FSC (resolution estimation) | emd_72930_fsc.xml | 8.4 KB | Display | FSC data file |
| Images | emd_72930.png | 31 KB | ||
| Filedesc metadata | emd-72930.cif.gz | 4.2 KB | ||
| Others | emd_72930_half_map_1.map.gz emd_72930_half_map_2.map.gz | 59.5 MB 59.5 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-72930 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-72930 | 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_72930.map.gz / Format: CCP4 / Size: 64 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Local Refined C-terminus of PfRON5 | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.823 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: Half map A of Local Refined C-terminus of PfRON5
| File | emd_72930_half_map_1.map | ||||||||||||
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| Annotation | Half map A of Local Refined C-terminus of PfRON5 | ||||||||||||
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| Density Histograms |
-Half map: Half map B of Local Refined C-terminus of PfRON5
| File | emd_72930_half_map_2.map | ||||||||||||
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| Annotation | Half map B of Local Refined C-terminus of PfRON5 | ||||||||||||
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| Density Histograms |
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Sample components
-Entire : Plasmodium falciparum moving junction staple with PfAMA1 - PfRON2...
| Entire | Name: Plasmodium falciparum moving junction staple with PfAMA1 - PfRON2 - PfRON4 - PfRON5 |
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| Components |
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-Supramolecule #1: Plasmodium falciparum moving junction staple with PfAMA1 - PfRON2...
| Supramolecule | Name: Plasmodium falciparum moving junction staple with PfAMA1 - PfRON2 - PfRON4 - PfRON5 type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1-#4 |
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| Source (natural) | Organism: ![]() |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Buffer | pH: 7 |
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| Grid | Model: Quantifoil / Material: GOLD / Mesh: 300 / Support film - Material: CARBON / Support film - topology: HOLEY / Support film - Film thickness: 0.2 / Pretreatment - Type: GLOW DISCHARGE |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: GATAN K3 BIOCONTINUUM (6k x 4k) / Average electron dose: 58.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 3.0 µm / Nominal defocus min: 1.5 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
-Atomic model buiding 1
| Refinement | Protocol: AB INITIO MODEL |
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About Yorodumi



Keywords
Authors
United States, 1 items
Citation




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FIELD EMISSION GUN

