9fje

Expanded formalin inactivated CVB1

Method: ELECTRON MICROSCOPY Dmax: 100.3 Å Quality: GOOD

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

Capsid protein VP1

OrganismNot specified

UniProt A0A7T7KAA0

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein homooligomer Homooligomer Protein × 180 PDB declaration: 180-meric(180) Consistent with protein copy count Chain 1; UniProt 628–847 Chain 2; UniProt 81–329 Chain 3; UniProt 333–564 Not recorded No other associated polymer ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.01 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.

3 other PDB entries and 11 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A7T7KAA0_9ENTO
Isoform
PDB entities 1, 2, 3
Chains and sequence ranges Author chain 1; PDBConstruct 1–220; UniProt 628–847 Author chain 2; PDBConstruct 1–249; UniProt 81–329 Author chain 3; PDBConstruct 1–232; UniProt 333–564

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 9fje

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9fje
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9fje
Deposition date deposition_date2024-05-31
Structure title titleExpanded formalin inactivated CVB1
Keywords keywordscoxsackievirus B1, vaccine, formalin, VIRUS; VIRUS
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier29.55
Radius of gyration Rg (electron density) rg_electron28.73
Forward intensity I(0) i093060600.00
Molecular weight molecular_weight76284.0 kDa
Excluded volume excluded_volume95409 ų
Envelope volume envelope_volume117770 ų
Hydration-shell volume shell_volume34681 ų
Envelope diameter envelope_diameter106.2
Shell Rg shell_rg35.37
Envelope Rg envelope_rg29.54
Shape Rg shape_rg28.72
Total Rg total_rg29.39
Total atoms total_atoms5361
Residues n_residues685
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 dmax100.3
Rg (real space) rg_real29.61
Rg uncertainty (real space) rg_real_error0.86
I(0) (real space) i0_real9.3060e+07
I(0) uncertainty (real space) i0_real_error1.4610e+06
Rg (reciprocal space) rg_reciprocal29.59
I(0) (reciprocal space) i0_reciprocal93060000.0000
Solution quality estimate total_estimate0.8733
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary98.4
Skewness Skewness skewness0.455
Kurtosis Kurtosis kurtosis-0.142
Angular range angular_range— – 0.2700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha18310000.0000
Real-space data points n_real_points55
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.817; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.984; Smooth: 0.915

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)