6zxj

Fully-loaded anthrax lethal toxin in its heptameric pre-pore state, in which the third lethal factor is masked out (PA7LF3-masked)

Method: ELECTRON MICROSCOPY Dmax: 205.5 Å Quality: GOOD

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

Protective antigen

Bacillus anthracis

UniProt Q68GS1

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 heterocomplex Heteromer Protein × 9 PDB declaration: nonameric(9) Consistent with protein copy count Chain A; UniProt 1–736 Chain B; UniProt 1–736 Chain C; UniProt 1–736 Chain D; UniProt 1–736 Chain E; UniProt 1–736 Chain F; UniProt 1–736 Chain G; UniProt 1–736 Not recorded Lethal factor × 2 (P15917) ELECTRON MICROSCOPY cryo-EM buffer:pH 8.5 cryo-EM vitrification conditions:Cryogen ETHANE;4 uL sample was applied to grid (with 2 nm additional carbon layer) and incubated for 45 s prior blotting. Resolution 3.50 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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q68GS1_BACAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 24–759; UniProt 1–736 Author chain B; PDBConstruct 24–759; UniProt 1–736 Author chain C; PDBConstruct 24–759; UniProt 1–736 Author chain D; PDBConstruct 24–759; UniProt 1–736 Author chain E; PDBConstruct 24–759; UniProt 1–736 Author chain F; PDBConstruct 24–759; UniProt 1–736 Author chain G; PDBConstruct 24–759; UniProt 1–736

Lethal factor

Bacillus anthracis

UniProt P15917

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 heterocomplex Heteromer Protein × 9 PDB declaration: nonameric(9) Consistent with protein copy count Chain H; UniProt 1–809 Chain I; UniProt 1–809 Not recorded Protective antigen × 7 (Q68GS1) ELECTRON MICROSCOPY cryo-EM buffer:pH 8.5 cryo-EM vitrification conditions:Cryogen ETHANE;4 uL sample was applied to grid (with 2 nm additional carbon layer) and incubated for 45 s prior blotting. Resolution 3.50 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.

30 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LEF_BACAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain H; PDBConstruct 1–809; UniProt 1–809 Author chain I; PDBConstruct 1–809; UniProt 1–809

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 6zxj

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6zxj
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id6zxj
Deposition date deposition_date2020-07-29
Structure title titleFully-loaded anthrax lethal toxin in its heptameric pre-pore state, in which the third lethal factor is masked out (PA7LF3-masked)
Keywords keywordsanthrax lethal toxin, fully-loaded pre-pore state, membrane translocase, cytotoxic substrate, TOXIN; TOXIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier62.21
Radius of gyration Rg (electron density) rg_electron61.47
Forward intensity I(0) i04252480000.00
Molecular weight molecular_weight540930.0 kDa
Excluded volume excluded_volume672910 ų
Envelope volume envelope_volume1139600 ų
Hydration-shell volume shell_volume148700 ų
Envelope diameter envelope_diameter209.0
Shell Rg shell_rg68.32
Envelope Rg envelope_rg60.16
Shape Rg shape_rg61.52
Total Rg total_rg61.44
Total atoms total_atoms38244
Residues n_residues5099
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 dmax205.5
Rg (real space) rg_real61.88
Rg uncertainty (real space) rg_real_error1.79
I(0) (real space) i0_real4.2520e+09
I(0) uncertainty (real space) i0_real_error9.8680e+07
Rg (reciprocal space) rg_reciprocal62.47
I(0) (reciprocal space) i0_reciprocal4257000000.0000
Solution quality estimate total_estimate0.8726
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary82.2
Skewness Skewness skewness0.154
Kurtosis Kurtosis kurtosis-0.418
Angular range angular_range— – 0.1250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha385000000.0000
Real-space data points n_real_points26
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.855; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.952; Smooth: 0.822

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)