8zui

Binary cluster of TNF-TNFR1 ectodomain complex

Method: ELECTRON MICROSCOPY Dmax: 149.4 Å Quality: GOOD

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

Tumor necrosis factor

Homo sapiens

UniProt P01375

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 × 12 PDB declaration: 12-meric(12) Consistent with protein copy count Chain A; UniProt 77–233 Chain B; UniProt 77–233 Chain C; UniProt 77–233 Chain G; UniProt 77–233 Chain H; UniProt 77–233 Chain I; UniProt 77–233 Not recorded Tumor necrosis factor receptor superfamily member 1A, membrane form × 6 (P19438) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.56 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.

49 other PDB entries and 98 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TNFA_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–160; UniProt 77–233 Author chain B; PDBConstruct 4–160; UniProt 77–233 Author chain C; PDBConstruct 4–160; UniProt 77–233 Author chain G; PDBConstruct 4–160; UniProt 77–233 Author chain H; PDBConstruct 4–160; UniProt 77–233 Author chain I; PDBConstruct 4–160; UniProt 77–233

Tumor necrosis factor receptor superfamily member 1A, membrane form

Homo sapiens

UniProt P19438

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 × 12 PDB declaration: 12-meric(12) Consistent with protein copy count Chain D; UniProt 30–211 Chain E; UniProt 30–211 Chain F; UniProt 30–211 Chain J; UniProt 30–211 Chain K; UniProt 30–211 Chain L; UniProt 30–211 Not recorded Tumor necrosis factor × 6 (P01375) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.56 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 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TNR1A_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain D; PDBConstruct 4–185; UniProt 30–211 Author chain E; PDBConstruct 4–185; UniProt 30–211 Author chain F; PDBConstruct 4–185; UniProt 30–211 Author chain J; PDBConstruct 4–185; UniProt 30–211 Author chain K; PDBConstruct 4–185; UniProt 30–211 Author chain L; PDBConstruct 4–185; UniProt 30–211

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 8zui

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8zui
Deposition date deposition_date2024-06-09
Structure title titleBinary cluster of TNF-TNFR1 ectodomain complex
Keywords keywordsTNF receptor, Receptor, Receptor cluster, IMMUNE SYSTEM; IMMUNE SYSTEM
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier45.95
Radius of gyration Rg (electron density) rg_electron45.47
Forward intensity I(0) i0596471000.00
Molecular weight molecular_weight191460.0 kDa
Excluded volume excluded_volume235390 ų
Envelope volume envelope_volume340870 ų
Hydration-shell volume shell_volume62617 ų
Envelope diameter envelope_diameter155.3
Shell Rg shell_rg49.20
Envelope Rg envelope_rg45.17
Shape Rg shape_rg45.41
Total Rg total_rg45.82
Total atoms total_atoms13378
Residues n_residues1722
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 dmax149.4
Rg (real space) rg_real46.09
Rg uncertainty (real space) rg_real_error1.30
I(0) (real space) i0_real5.9650e+08
I(0) uncertainty (real space) i0_real_error1.1230e+07
Rg (reciprocal space) rg_reciprocal45.95
I(0) (reciprocal space) i0_reciprocal596400000.0000
Solution quality estimate total_estimate0.8665
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary48.3
Skewness Skewness skewness0.356
Kurtosis Kurtosis kurtosis-0.604
Angular range angular_range— – 0.1700 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha43140000.0000
Real-space data points n_real_points35
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.887; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.993; Smooth: 0.606

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)