7vpp

Structures of a deltacoronavirus spike protein bound to porcine and human receptors indicate the risk of virus adaptation to humans

Method: X-RAY DIFFRACTION Dmax: 142.5 Å Quality: GOOD

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

Aminopeptidase

Sus scrofa

UniProt K7GMF9

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 Heteromer Protein × 3 其他Polymer 10 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 58–961 Chain C; UniProt 58–961 Not recorded Spike protein × 1 (A0A4P8D758) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 9 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 ZN ZINC ION × 2 GOL GLYCEROL × 5 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 5 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;291.15 K;solution containing 8% w/v Polyethylene glycol 1000, 8% w/v Polyethylene glycol 8000 and 20% w/v Glycerol Resolution 2.69 Å R-free 0.230

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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name K7GMF9_PIG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–904; UniProt 58–961 Author chain C; PDBConstruct 1–904; UniProt 58–961

Spike protein

Porcine deltacoronavirus

UniProt A0A4P8D758

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 Heteromer Protein × 3 其他Polymer 10 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 299–418 Not recorded Aminopeptidase × 2 (K7GMF9) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 9 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-3)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 ZN ZINC ION × 2 GOL GLYCEROL × 5 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 5 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;291.15 K;solution containing 8% w/v Polyethylene glycol 1000, 8% w/v Polyethylene glycol 8000 and 20% w/v Glycerol Resolution 2.69 Å R-free 0.230

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.

1 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A4P8D758_9NIDO
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–120; UniProt 299–418

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 7vpp

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7vpp
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7vpp
Deposition date deposition_date2021-10-17
Structure title titleStructures of a deltacoronavirus spike protein bound to porcine and human receptors indicate the risk of virus adaptation to humans
Keywords keywordsPorcine Deltacoronavirus, receptor, cross-species transmission, VIRAL PROTEIN, HYDROLASE-VIRAL PROTEIN complex; HYDROLASE/VIRAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier43.53
Radius of gyration Rg (electron density) rg_electron43.27
Forward intensity I(0) i0709964000.00
Molecular weight molecular_weight221070.0 kDa
Excluded volume excluded_volume276650 ų
Envelope volume envelope_volume360510 ų
Hydration-shell volume shell_volume69238 ų
Envelope diameter envelope_diameter150.1
Shell Rg shell_rg48.50
Envelope Rg envelope_rg42.84
Shape Rg shape_rg43.24
Total Rg total_rg43.61
Total atoms total_atoms15580
Residues n_residues1892
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 dmax142.5
Rg (real space) rg_real43.54
Rg uncertainty (real space) rg_real_error1.26
I(0) (real space) i0_real7.1000e+08
I(0) uncertainty (real space) i0_real_error1.3620e+07
Rg (reciprocal space) rg_reciprocal43.53
I(0) (reciprocal space) i0_reciprocal710000000.0000
Solution quality estimate total_estimate0.8903
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary43.5
Skewness Skewness skewness0.292
Kurtosis Kurtosis kurtosis-0.624
Angular range angular_range— – 0.1800 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha138500000.0000
Real-space data points n_real_points37
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.892; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.902

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

8. Citations (1)

9. Files and Curves (10)