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Yorodumi- PDB-8yf2: Cryo-EM structure of SARS-CoV-2 prototype RBD in complex with rac... -
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Open data
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Basic information
| Entry | Database: PDB / ID: 8yf2 | ||||||
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| Title | Cryo-EM structure of SARS-CoV-2 prototype RBD in complex with raccoon dog ACE2 (local refinement) | ||||||
Components |
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Keywords | VIRAL PROTEIN/HYDROLASE / SARS-CoV-2 / rototype RBD / raccoon dog / ACE2 / VIRAL PROTEIN-HYDROLASE Complex | ||||||
| Function / homology | Function and homology informationHydrolases; Acting on peptide bonds (peptidases) / peptidyl-dipeptidase activity / carboxypeptidase activity / metallopeptidase activity / symbiont-mediated disruption of host tissue / Maturation of spike protein / Translation of Structural Proteins / Virion Assembly and Release / host cell surface / host extracellular space ...Hydrolases; Acting on peptide bonds (peptidases) / peptidyl-dipeptidase activity / carboxypeptidase activity / metallopeptidase activity / symbiont-mediated disruption of host tissue / Maturation of spike protein / Translation of Structural Proteins / Virion Assembly and Release / host cell surface / host extracellular space / viral translation / symbiont-mediated-mediated suppression of host tetherin activity / Induction of Cell-Cell Fusion / structural constituent of virion / entry receptor-mediated virion attachment to host cell / membrane fusion / Attachment and Entry / host cell endoplasmic reticulum-Golgi intermediate compartment membrane / positive regulation of viral entry into host cell / receptor-mediated virion attachment to host cell / host cell surface receptor binding / cilium / symbiont-mediated suppression of host innate immune response / apical plasma membrane / receptor ligand activity / endocytosis involved in viral entry into host cell / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / symbiont entry into host cell / virion attachment to host cell / SARS-CoV-2 activates/modulates innate and adaptive immune responses / host cell plasma membrane / virion membrane / proteolysis / extracellular space / metal ion binding / identical protein binding / membrane / plasma membrane / cytoplasm Similarity search - Function | ||||||
| Biological species | ![]() ![]() | ||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 2.64 Å | ||||||
Authors | Li, L.J. / Luo, C.L. / Qi, J.X. / Gao, G.F. | ||||||
| Funding support | China, 1items
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Citation | Journal: PLoS Pathog / Year: 2024Title: Receptor binding and structural basis of raccoon dog ACE2 binding to SARS-CoV-2 prototype and its variants. Authors: Chunliang Luo / Linjie Li / Yuhang Gu / Hangchuan Zhang / Zepeng Xu / Junqing Sun / Kaiyuan Shi / Sufang Ma / Wen-Xia Tian / Kefang Liu / George F Gao / ![]() Abstract: Raccoon dog was proposed as a potential host of SARS-CoV-2, but no evidence support such a notion. In our study, we investigated the binding affinities of raccoon dog ACE2 (rdACE2) to the spike (S) ...Raccoon dog was proposed as a potential host of SARS-CoV-2, but no evidence support such a notion. In our study, we investigated the binding affinities of raccoon dog ACE2 (rdACE2) to the spike (S) protein receptor binding domain (RBD) of SARS-CoV-2 prototype (PT) and its variants. It revealed that the binding affinities of RBD from SARS-CoV-2 variants were generally lower than that of the PT RBD. Through structural and functional analyses, we found amino acids H34 and M82 play pivotal roles in maintaining the binding affinity of ACE2 to different SARS-CoV-2 sub-variants. These results suggest that raccoon dogs exhibit lower susceptibility to SARS-CoV-2 compared to those animal species with a high prevalence of SARS-CoV-2 transmission. | ||||||
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Structure visualization
| Structure viewer | Molecule: Molmil Jmol/JSmol |
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Downloads & links
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Download
| PDBx/mmCIF format | 8yf2.cif.gz | 175.8 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8yf2.ent.gz | 135.1 KB | Display | PDB format |
| PDBx/mmJSON format | 8yf2.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Summary document | 8yf2_validation.pdf.gz | 1.6 MB | Display | wwPDB validaton report |
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| Full document | 8yf2_full_validation.pdf.gz | 1.6 MB | Display | |
| Data in XML | 8yf2_validation.xml.gz | 40.3 KB | Display | |
| Data in CIF | 8yf2_validation.cif.gz | 55.8 KB | Display | |
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/yf/8yf2 ftp://data.pdbj.org/pub/pdb/validation_reports/yf/8yf2 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 39208MC ![]() 8yftC M: map data used to model this data C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
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Assembly
| Deposited unit | ![]()
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Components
| #1: Protein | Mass: 25951.219 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Gene: S, 2 / Production host: Homo sapiens (human) / References: UniProt: P0DTC2 | ||||||||
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| #2: Protein | Mass: 70600.086 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human)References: UniProt: B4XEP4, Hydrolases; Acting on peptide bonds (peptidases) | ||||||||
| #3: Polysaccharide | 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose Source method: isolated from a genetically manipulated source #4: Chemical | ChemComp-ZN / | #5: Sugar | ChemComp-NAG / | Has ligand of interest | Y | Has protein modification | Y | |
-Experimental details
-Experiment
| Experiment | Method: ELECTRON MICROSCOPY |
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| EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
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Sample preparation
| Component | Name: SARS-CoV-2 prototype spike in complex with raccoon dog ACE2 Type: COMPLEX / Entity ID: #1-#2 / Source: RECOMBINANT |
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| Source (natural) | Organism: ![]() |
| Source (recombinant) | Organism: Homo sapiens (human) |
| Buffer solution | pH: 8 |
| Specimen | Embedding applied: NO / Shadowing applied: NO / Staining applied: NO / Vitrification applied: YES |
| Vitrification | Cryogen name: ETHANE |
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Electron microscopy imaging
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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| Microscopy | Model: TFS KRIOS |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2000 nm / Nominal defocus min: 1000 nm |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K3 (6k x 4k) |
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Processing
| EM software | Name: PHENIX / Version: 1.20.1_4487: / Category: model refinement | ||||||||||||||||||||||||
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| CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION | ||||||||||||||||||||||||
| 3D reconstruction | Resolution: 2.64 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 392889 / Symmetry type: POINT | ||||||||||||||||||||||||
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About Yorodumi






China, 1items
Citation




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Homo sapiens (human)


FIELD EMISSION GUN