3j2j

Empty coxsackievirus A9 capsid

Method: ELECTRON MICROSCOPY Dmax: 97.6 Å Quality: GOOD

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

Protein VP1

OrganismNot specified

UniProt P21404

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 A; UniProt 631–852 Chain B; UniProt 331–568 Chain C; UniProt 79–330 Fragment:UNP residues 631-852 Fragment:UNP residues 331-568 Fragment:UNP residues 79-330 No other associated polymer ELECTRON MICROSCOPY cryo-EM vitrification conditions:manual plunging;Cryogen ETHANE;manual plunging into liquid ethane (GATAN CRYOPLUNGE 3) Resolution 9.54 Å
2 Protein homooligomer Homooligomer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 631–852 Chain B; UniProt 331–568 Chain C; UniProt 79–330 Fragment:UNP residues 631-852 Fragment:UNP residues 331-568 Fragment:UNP residues 79-330 No other associated polymer ELECTRON MICROSCOPY cryo-EM vitrification conditions:manual plunging;Cryogen ETHANE;manual plunging into liquid ethane (GATAN CRYOPLUNGE 3) Resolution 9.54 Å
3 Protein homooligomer Homooligomer Protein × 15 PDB declaration: pentadecameric(15) Consistent with protein copy count Chain A; UniProt 631–852 Chain B; UniProt 331–568 Chain C; UniProt 79–330 Fragment:UNP residues 631-852 Fragment:UNP residues 331-568 Fragment:UNP residues 79-330 No other associated polymer ELECTRON MICROSCOPY cryo-EM vitrification conditions:manual plunging;Cryogen ETHANE;manual plunging into liquid ethane (GATAN CRYOPLUNGE 3) Resolution 9.54 Å
4 Protein homooligomer Homooligomer Protein × 18 PDB declaration: octadecameric(18) Consistent with protein copy count Chain A; UniProt 631–852 Chain B; UniProt 331–568 Chain C; UniProt 79–330 Fragment:UNP residues 631-852 Fragment:UNP residues 331-568 Fragment:UNP residues 79-330 No other associated polymer ELECTRON MICROSCOPY cryo-EM vitrification conditions:manual plunging;Cryogen ETHANE;manual plunging into liquid ethane (GATAN CRYOPLUNGE 3) Resolution 9.54 Å
5 Protein homooligomer Homooligomer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 631–852 Chain B; UniProt 331–568 Chain C; UniProt 79–330 Fragment:UNP residues 631-852 Fragment:UNP residues 331-568 Fragment:UNP residues 79-330 No other associated polymer ELECTRON MICROSCOPY cryo-EM vitrification conditions:manual plunging;Cryogen ETHANE;manual plunging into liquid ethane (GATAN CRYOPLUNGE 3) Resolution 9.54 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.

12 other PDB entries and 17 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name POLG_CXA9
Isoform
PDB entities 1, 2, 3
Chains and sequence ranges Author chain A; PDBConstruct 1–222; UniProt 631–852 Author chain B; PDBConstruct 1–238; UniProt 331–568 Author chain C; PDBConstruct 1–252; UniProt 79–330

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 3j2j

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3j2j
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3j2j
Deposition date deposition_date2012-10-04
Structure title titleEmpty coxsackievirus A9 capsid
Keywords keywordsCVA9-integrin, picornavirus, enterovirus, empty capsid, VIRUS; VIRUS
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier29.82
Radius of gyration Rg (electron density) rg_electron28.98
Forward intensity I(0) i0103240000.00
Molecular weight molecular_weight79707.0 kDa
Excluded volume excluded_volume99491 ų
Envelope volume envelope_volume126830 ų
Hydration-shell volume shell_volume36677 ų
Envelope diameter envelope_diameter102.3
Shell Rg shell_rg36.03
Envelope Rg envelope_rg29.43
Shape Rg shape_rg28.97
Total Rg total_rg29.69
Total atoms total_atoms5601
Residues n_residues712
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 dmax97.6
Rg (real space) rg_real29.81
Rg uncertainty (real space) rg_real_error0.74
I(0) (real space) i0_real1.0320e+08
I(0) uncertainty (real space) i0_real_error1.5380e+06
Rg (reciprocal space) rg_reciprocal29.82
I(0) (reciprocal space) i0_reciprocal103200000.0000
Solution quality estimate total_estimate0.8900
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary35.0
Skewness Skewness skewness0.351
Kurtosis Kurtosis kurtosis-0.311
Angular range angular_range— – 0.2650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha22420000.0000
Real-space data points n_real_points54
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.888; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.996; Smooth: 0.907

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)