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Open data
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Basic information
| Entry | Database: PDB / ID: 8xz8 | |||||||||||||||||||||||||||||||||
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| Title | BA.2.86 Spike in complex with bovine ACE2 (bound 1 ACE2) | |||||||||||||||||||||||||||||||||
Components |
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Keywords | VIRAL PROTEIN / SARS-CoV-2 / complex / Spike | |||||||||||||||||||||||||||||||||
| 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 / viral translation ...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 / viral translation / host extracellular space / symbiont-mediated-mediated suppression of host tetherin activity / Induction of Cell-Cell Fusion / structural constituent of virion / membrane fusion / entry receptor-mediated virion attachment to host cell / 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 region / metal ion binding / identical protein binding / membrane / plasma membrane / cytoplasm Similarity search - Function | |||||||||||||||||||||||||||||||||
| Biological species | ![]() ![]() | |||||||||||||||||||||||||||||||||
| Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.65 Å | |||||||||||||||||||||||||||||||||
Authors | Yue, C. / Liu, P. | |||||||||||||||||||||||||||||||||
| Funding support | 1items
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Citation | Journal: To Be PublishedTitle: BA.2.86 Spike in complex with bovine ACE2 Authors: Yue, C. / Liu, P. | |||||||||||||||||||||||||||||||||
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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 | 8xz8.cif.gz | 694.4 KB | Display | PDBx/mmCIF format |
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| PDB format | pdb8xz8.ent.gz | 564.2 KB | Display | PDB format |
| PDBx/mmJSON format | 8xz8.json.gz | Tree view | PDBx/mmJSON format | |
| Others | Other downloads |
-Validation report
| Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/xz/8xz8 ftp://data.pdbj.org/pub/pdb/validation_reports/xz/8xz8 | HTTPS FTP |
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-Related structure data
| Related structure data | ![]() 38789MC ![]() 8xz9C ![]() 8xzaC 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
-Protein , 2 types, 4 molecules ABCD
| #1: Protein | Mass: 93201.109 Da / Num. of mol.: 1 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Homo sapiens (human)References: UniProt: Q2HJI5, Hydrolases; Acting on peptide bonds (peptidases) |
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| #2: Protein | Mass: 134041.156 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) ![]() Strain: Omicron/BA.2.86 / Gene: S, 2 / Production host: Homo sapiens (human) / References: UniProt: P0DTC2 |
-Sugars , 2 types, 53 molecules 
| #3: Polysaccharide | beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose Source method: isolated from a genetically manipulated source #6: Sugar | ChemComp-NAG / |
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-Non-polymers , 2 types, 2 molecules 


| #4: Chemical | ChemComp-ZN / |
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| #5: Chemical | ChemComp-CL / |
-Details
| Has ligand of interest | N |
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| 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: BA.2.86 Spike in complex with bovine ACE2 / Type: COMPLEX / Entity ID: #2, #1 / Source: RECOMBINANT | ||||||||||||
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| Source (natural) |
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| Source (recombinant) | Organism: Homo sapiens (human) | ||||||||||||
| Buffer solution | pH: 7.4 | ||||||||||||
| 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: Talos Arctica / Image courtesy: FEI Company |
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| Microscopy | Model: FEI TALOS ARCTICA |
| Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 200 kV / Illumination mode: FLOOD BEAM |
| Electron lens | Mode: DARK FIELD / Nominal defocus max: 2000 nm / Nominal defocus min: 1200 nm |
| Image recording | Electron dose: 60 e/Å2 / Film or detector model: GATAN K2 SUMMIT (4k x 4k) |
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Processing
| EM software | Name: PHENIX / Category: model refinement |
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| CTF correction | Type: PHASE FLIPPING ONLY |
| 3D reconstruction | Resolution: 3.65 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 89392 / Symmetry type: POINT |
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Homo sapiens (human)
FIELD EMISSION GUN