+Open data
-Basic information
Entry | Database: PDB / ID: 8y1h | ||||||
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Title | The 2up formation of the HKU1-B S protein in the apo state | ||||||
Components | Spike glycoprotein | ||||||
Keywords | VIRAL PROTEIN / HCoV-HKU1 | ||||||
Function / homology | Function and homology information endocytosis involved in viral entry into host cell / host cell endoplasmic reticulum-Golgi intermediate compartment membrane / receptor-mediated virion attachment to host cell / fusion of virus membrane with host plasma membrane / fusion of virus membrane with host endosome membrane / viral envelope / host cell plasma membrane / virion membrane / membrane Similarity search - Function | ||||||
Biological species | Human coronavirus HKU1 | ||||||
Method | ELECTRON MICROSCOPY / single particle reconstruction / cryo EM / Resolution: 3.16 Å | ||||||
Authors | Xia, L.Y. / Zhang, Y.Y. / Zhou, Q. | ||||||
Funding support | China, 1items
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Citation | Journal: Cell Res / Year: 2024 Title: Structural basis for the recognition of HCoV-HKU1 by human TMPRSS2. Authors: Lingyun Xia / Yuanyuan Zhang / Qiang Zhou / | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 8y1h.cif.gz | 658 KB | Display | PDBx/mmCIF format |
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PDB format | pdb8y1h.ent.gz | 538.5 KB | Display | PDB format |
PDBx/mmJSON format | 8y1h.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 8y1h_validation.pdf.gz | 2.2 MB | Display | wwPDB validaton report |
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Full document | 8y1h_full_validation.pdf.gz | 2.3 MB | Display | |
Data in XML | 8y1h_validation.xml.gz | 72.8 KB | Display | |
Data in CIF | 8y1h_validation.cif.gz | 111.1 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/y1/8y1h ftp://data.pdbj.org/pub/pdb/validation_reports/y1/8y1h | HTTPS FTP |
-Related structure data
Related structure data | 38836MC 8y19C 8y1aC 8y1bC 8y1cC 8y1dC 8y1eC 8y1fC 8y1gC M: map data used to model this data C: citing same article (ref.) |
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Similar structure data | Similarity search - Function & homologyF&H Search |
-Links
-Assembly
Deposited unit |
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1 |
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-Components
#1: Protein | Mass: 143475.344 Da / Num. of mol.: 3 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Human coronavirus HKU1 (isolate N2) / Gene: S, 3 / Production host: Homo sapiens (human) / References: UniProt: Q14EB0 #2: Polysaccharide | Source method: isolated from a genetically manipulated source #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: Sugar | ChemComp-NAG / Has ligand of interest | Y | Has protein modification | Y | |
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-Experimental details
-Experiment
Experiment | Method: ELECTRON MICROSCOPY |
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EM experiment | Aggregation state: PARTICLE / 3D reconstruction method: single particle reconstruction |
-Sample preparation
Component | Name: The 2up formation of the HKU1-B S protein in the apo state Type: COMPLEX / Entity ID: #1 / Source: RECOMBINANT |
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Source (natural) | Organism: Human coronavirus HKU1 (isolate N2) |
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 |
-Electron microscopy imaging
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |
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Microscopy | Model: FEI TITAN KRIOS |
Electron gun | Electron source: FIELD EMISSION GUN / Accelerating voltage: 300 kV / Illumination mode: FLOOD BEAM |
Electron lens | Mode: BRIGHT FIELD / Nominal defocus max: 2200 nm / Nominal defocus min: 1200 nm / Alignment procedure: COMA FREE |
Specimen holder | Cryogen: NITROGEN / Specimen holder model: FEI TITAN KRIOS AUTOGRID HOLDER |
Image recording | Electron dose: 50 e/Å2 / Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) |
-Processing
EM software | Name: cryoSPARC / Version: 4 / Category: 3D reconstruction |
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CTF correction | Type: PHASE FLIPPING AND AMPLITUDE CORRECTION |
3D reconstruction | Resolution: 3.16 Å / Resolution method: FSC 0.143 CUT-OFF / Num. of particles: 134669 / Symmetry type: POINT |