8s2n

Xenorhabdus bovienii Rhs toxin TreTu complex with TrxA and TriTu immunity protein

Method: X-RAY DIFFRACTION Dmax: 87.8 Å Quality: REASONABLE

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

Immunity Protein TriX

Xenorhabdus bovienii SS-2004

UniProt D3UXR2

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–134 Not recorded Complete genome segment 11/17 × 1 (D3UXR3) Thioredoxin 1 × 1 (P0AA25) PEG DI(HYDROXYETHYL)ETHER × 3 SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M Ammonium sulfate, 0.02 M Sodium chloride, 0.02 M Sodium acetate pH 4.0, 33 % v/v PEG 200 Resolution 2.11 Å R-free 0.232

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 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name D3UXR2_XENBS
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–134; UniProt 1–134

Complete genome segment 11/17

Xenorhabdus bovienii SS-2004

UniProt D3UXR3

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain B; UniProt 1380–1518 Not recorded Immunity Protein TriX × 1 (D3UXR2) Thioredoxin 1 × 1 (P0AA25) PEG DI(HYDROXYETHYL)ETHER × 3 SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M Ammonium sulfate, 0.02 M Sodium chloride, 0.02 M Sodium acetate pH 4.0, 33 % v/v PEG 200 Resolution 2.11 Å R-free 0.232

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 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name D3UXR3_XENBS
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 2–140; UniProt 1380–1518

Thioredoxin 1

Escherichia coli str. K-12 substr. MG1655

UniProt P0AA25

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 2–109 Not recorded Immunity Protein TriX × 1 (D3UXR2) Complete genome segment 11/17 × 1 (D3UXR3) PEG DI(HYDROXYETHYL)ETHER × 3 SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293 K;0.2 M Ammonium sulfate, 0.02 M Sodium chloride, 0.02 M Sodium acetate pH 4.0, 33 % v/v PEG 200 Resolution 2.11 Å R-free 0.232

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.

52 other PDB entries and 100 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name THIO_ECOLI
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 4–111; UniProt 2–109

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 8s2n

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8s2n
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8s2n
Deposition date deposition_date2024-02-18
Structure title titleXenorhabdus bovienii Rhs toxin TreTu complex with TrxA and TriTu immunity protein
Keywords keywordsADP-ribosyltransferase, thioredoxin, TOXIN; TOXIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier24.88
Radius of gyration Rg (electron density) rg_electron24.65
Forward intensity I(0) i029809800.00
Molecular weight molecular_weight42014.0 kDa
Excluded volume excluded_volume52552 ų
Envelope volume envelope_volume62824 ų
Hydration-shell volume shell_volume22600 ų
Envelope diameter envelope_diameter90.7
Shell Rg shell_rg30.46
Envelope Rg envelope_rg25.13
Shape Rg shape_rg24.65
Total Rg total_rg25.35
Total atoms total_atoms2953
Residues n_residues372
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 dmax87.8
Rg (real space) rg_real25.14
Rg uncertainty (real space) rg_real_error0.88
I(0) (real space) i0_real2.9810e+07
I(0) uncertainty (real space) i0_real_error5.0700e+05
Rg (reciprocal space) rg_reciprocal25.08
I(0) (reciprocal space) i0_reciprocal29810000.0000
Solution quality estimate total_estimate0.7062
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary22.3
Skewness Skewness skewness0.567
Kurtosis Kurtosis kurtosis-0.277
Angular range angular_range— – 0.3200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha18040000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.538; Stabil: 0.979; Sysdev: 1.000; Positv: 1.000; Valcen: 0.625; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)