3j9c

CryoEM single particle reconstruction of anthrax toxin protective antigen pore at 2.9 Angstrom resolution

Method: ELECTRON MICROSCOPY Dmax: 197.9 Å Quality: REASONABLE

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

Protective antigen PA-63

Bacillus anthracis

UniProt P13423

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 × 7 PDB declaration: 7-MERIC(7) Consistent with protein copy count Chain A; UniProt 203–764 Fragment:C-terminal 63-kDa fragment (UNP residues 203-764) CA CALCIUM ION × 14 ELECTRON MICROSCOPY cryo-EM buffer:50 mM NaOAc, pH 5.0, 0.05% Igepal CA-630;pH 5;50 mM NaOAc, pH 5.0, 0.05% Igepal CA-630 cryo-EM vitrification conditions:Cryogen ETHANE;Plunged into liguid nitrogen (FEI VITROBOT MARK IV). Resolution 2.90 Å
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 203–764 Fragment:C-terminal 63-kDa fragment (UNP residues 203-764) CA CALCIUM ION × 2 ELECTRON MICROSCOPY cryo-EM buffer:50 mM NaOAc, pH 5.0, 0.05% Igepal CA-630;pH 5;50 mM NaOAc, pH 5.0, 0.05% Igepal CA-630 cryo-EM vitrification conditions:Cryogen ETHANE;Plunged into liguid nitrogen (FEI VITROBOT MARK IV). Resolution 2.90 Å
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 203–764 Fragment:C-terminal 63-kDa fragment (UNP residues 203-764) CA CALCIUM ION × 2 ELECTRON MICROSCOPY cryo-EM buffer:50 mM NaOAc, pH 5.0, 0.05% Igepal CA-630;pH 5;50 mM NaOAc, pH 5.0, 0.05% Igepal CA-630 cryo-EM vitrification conditions:Cryogen ETHANE;Plunged into liguid nitrogen (FEI VITROBOT MARK IV). Resolution 2.90 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.

28 other PDB entries and 40 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PAG_BACAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–562; UniProt 203–764

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 3j9c

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3j9c
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3j9c
Deposition date deposition_date2014-12-25
Structure title titleCryoEM single particle reconstruction of anthrax toxin protective antigen pore at 2.9 Angstrom resolution
Keywords keywordsbacterial toxin, anthrax toxin, protective antigen, protein translocation channel, TOXIN, TRANSPORT PROTEIN; TOXIN, TRANSPORT PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier43.15
Radius of gyration Rg (electron density) rg_electron45.52
Forward intensity I(0) i037812500.00
Molecular weight molecular_weight47249.0 kDa
Excluded volume excluded_volume58686 ų
Envelope volume envelope_volume105890 ų
Hydration-shell volume shell_volume24210 ų
Envelope diameter envelope_diameter190.1
Shell Rg shell_rg36.39
Envelope Rg envelope_rg57.72
Shape Rg shape_rg45.63
Total Rg total_rg44.46
Total atoms total_atoms3328
Residues n_residues423
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 dmax197.9
Rg (real space) rg_real45.88
Rg uncertainty (real space) rg_real_error4.64
I(0) (real space) i0_real3.7810e+07
I(0) uncertainty (real space) i0_real_error8.9740e+05
Rg (reciprocal space) rg_reciprocal43.16
I(0) (reciprocal space) i0_reciprocal37690000.0000
Solution quality estimate total_estimate0.6104
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.7
Skewness Skewness skewness1.206
Kurtosis Kurtosis kurtosis0.525
Angular range angular_range— – 0.1850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2983000.0000
Real-space data points n_real_points38
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.000; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.000; Smooth: 0.929

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd3j9ca1
Class classb — All beta proteins
Fold Fold foldb.179 — Anthrax protective antigen N-terminal-like
Superfamily Superfamily superfamilyb.179.1 — PA14-like
Family Family familyb.179.1.1 — PA14

CATH v4.4 (1 domains)

Domain ID domain_id3j9cA03
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily110

8. Citations (1)

9. Files and Curves (10)