8jyk

Structure of the SARS-CoV-2 XBB.1.5 spike glycoprotein (closed state 1)

Method: ELECTRON MICROSCOPY Dmax: 150.7 Å Quality: REASONABLE

1. Protein Identity and Related Structures Protein Identity & Related Structures

Spike glycoprotein

Severe acute respiratory syndrome coronavirus 2

UniProt P0DTC2

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Homooligomer Protein × 3 其他Polymer 9 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 28–1210 Mutation:F817P, A892P, A899P, A942P, K986P, V987P, R682G, R683S, R685G 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 9 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 36 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE;blotting time 5 s and blotting force 5. Resolution 2.59 Å
2 Other combination Monomer Protein × 1 其他Polymer 3 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 28–1210 Mutation:F817P, A892P, A899P, A942P, K986P, V987P, R682G, R683S, R685G 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 12 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE;blotting time 5 s and blotting force 5. Resolution 2.59 Å
3 Other combination Monomer Protein × 1 其他Polymer 3 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 28–1210 Mutation:F817P, A892P, A899P, A942P, K986P, V987P, R682G, R683S, R685G 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 3 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 12 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE;blotting time 5 s and blotting force 5. Resolution 2.59 Å

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

2152 other PDB entries and 2471 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPIKE_SARS2
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 24–1205; UniProt 28–1210

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 8jyk

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8jyk
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8jyk
Deposition date deposition_date2023-07-03
Structure title titleStructure of the SARS-CoV-2 XBB.1.5 spike glycoprotein (closed state 1)
Keywords keywordsspike protein, glycoprotein, VIRUS, VIRAL PROTEIN; VIRAL PROTEIN
Experimental Method methodELECTRON MICROSCOPY

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier46.04
Radius of gyration Rg (electron density) rg_electron46.09
Forward intensity I(0) i0216412000.00
Molecular weight molecular_weight121270.0 kDa
Excluded volume excluded_volume152320 ų
Envelope volume envelope_volume248470 ų
Hydration-shell volume shell_volume48694 ų
Envelope diameter envelope_diameter158.0
Shell Rg shell_rg46.05
Envelope Rg envelope_rg44.66
Shape Rg shape_rg46.12
Total Rg total_rg45.96
Total atoms total_atoms8546
Residues n_residues1061
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax150.7
Rg (real space) rg_real46.25
Rg uncertainty (real space) rg_real_error1.47
I(0) (real space) i0_real2.1640e+08
I(0) uncertainty (real space) i0_real_error4.5850e+06
Rg (reciprocal space) rg_reciprocal46.05
I(0) (reciprocal space) i0_reciprocal216400000.0000
Solution quality estimate total_estimate0.6411
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary53.2
Skewness Skewness skewness0.374
Kurtosis Kurtosis kurtosis-0.374
Angular range angular_range— – 0.1700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8399000.0000
Real-space data points n_real_points35
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.885; Stabil: 1.000; Sysdev: 0.115; Positv: 1.000; Valcen: 0.987; Smooth: 0.343

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)