SAXSdb — 2eod

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

TNF receptor-associated factor 4

Homo sapiens

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 monomer Monomer Protein × 1 PDB declaration: monomeric（1） Consistent with protein copy count	Chain A； UniProt 190–248	Fragment：zf-TRAF, UNP residues 190-248	ZN ZINC ION × 2	SOLUTION NMR NMR measurement conditions：pH 7；293 K；Ionic strength (raw mmCIF value) 120mM；Pressure ambient NMR sample composition：1.13mM uniformly 13C,15N-labeled protein; 20mM TrisHCl; 100mM NaCl; 1mM DTT; 0.02% NaN3; 0.05mM ZnCl2; 1mM IDA; 10% D2O, 90% H2O \| 10% D2O, 90% H2O	Resolution not provided

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.

Other PDB	Difference from Current Entry 2EOD	Assembly / Oligomeric State	Construct	Mutations and Modifications	Ligands, Ions and Non-polymers	Method and Experimental Conditions	Structure Quality
2YUC Solution structure of the TRAF-type zinc finger domains (102-164) from human TNF receptor associated factor 4 Deposited 2007-04-06	Different construct Different experimental conditions	Assembly 1 Protein monomer Monomer；Protein × 1 PDB declaration: monomeric	Chain A 102–164（63 aa） Fragment：TRAF-type zinc finger domains	Not recorded	ZN ZINC ION × 2	SOLUTION NMR NMR measurement conditions pH 7；298 K；Ionic strength (raw mmCIF value) 120mM；Pressure ambient NMR sample composition 1.24mM U-15N, 13C-labeled protein; 20mM d-Tris-HCl; 100mM NaCl; 1mM DTT; 0.02% NaN3; 0.05mM ZnCl2; 1mM IDA, 90% H2O, 10%D2O \| 90% H2O/10% D2O	Resolution not provided
3ZJB The structure of the TRAF domain of human TRAF4 Deposited 2013-01-17	Different construct Different mutation/modification Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 1 Protein homooligomer Homooligomer；Protein × 3 PDB declaration: trimeric	Chain A 283–470（188 aa） Fragment：MATH DOMAIN, RESIDUES 283-470 Chain B 283–470（188 aa） Fragment：MATH DOMAIN, RESIDUES 283-470 Chain C 283–470（188 aa） Fragment：MATH DOMAIN, RESIDUES 283-470	Not recorded	CL CHLORIDE ION × 3	X-RAY DIFFRACTION X-ray crystallization conditions pH 7；15% PEG 4000, 0.1M HEPES PH 7.0	Resolution 1.84 Å R-free 0.200
4K8U Crystal structure of TRAF4 TRAF domain Deposited 2013-04-18	Different construct Different mutation/modification Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 1 Protein homooligomer Homooligomer；Protein × 3 PDB declaration: trimeric	Chain A 281–470（190 aa） Fragment：UNP residues 281-470 Chain B 281–470（190 aa） Fragment：UNP residues 281-470 Chain C 281–470（190 aa） Fragment：UNP residues 281-470	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；pH 7；298 K；13% PEG 3350, 0.14M Magnessium formate, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K	Resolution 2.30 Å R-free 0.281
4M4E TRAF domain of human TRAF4 Deposited 2013-08-07	Different construct Different mutation/modification Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 1 Protein homooligomer Homooligomer；Protein × 3 PDB declaration: trimeric	Chain A 292–466（175 aa） Chain B 292–466（175 aa） Chain C 292–466（175 aa）	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；pH 6.2；289 K；0.2M Ammonium fluoride, 20%(w/v) Polyethylene glycol 3350, pH 6.2, VAPOR DIFFUSION, HANGING DROP, temperature 289K	Resolution 2.60 Å R-free 0.277
5YC1 TRAF4_GPIb complex Deposited 2017-09-06	Different construct Different mutation/modification Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 1 Protein heterocomplex Heteromer；Protein × 4 PDB declaration: tetrameric	Chain A 290–470（181 aa） Fragment：UNP residues 290-470 Chain B 290–470（181 aa） Fragment：UNP residues 290-470 Chain C 290–470（181 aa） Fragment：UNP residues 290-470	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；298 K；magnesium formate dehydrate, polyethylene glycol 3350	Resolution 2.51 Å R-free 0.265
5YC1 TRAF4_GPIb complex Deposited 2017-09-06	Different construct Different mutation/modification Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 2 Protein heterocomplex Heteromer；Protein × 5 PDB declaration: pentameric	Chain D 290–470（181 aa） Fragment：UNP residues 290-470 Chain E 290–470（181 aa） Fragment：UNP residues 290-470 Chain F 290–470（181 aa） Fragment：UNP residues 290-470	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；298 K；magnesium formate dehydrate, polyethylene glycol 3350	Resolution 2.51 Å R-free 0.265
9OGV Identification of ligands for E3 ligases using fragment-based methods Deposited 2025-05-02	Different construct Different mutation/modification Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 1 Protein homooligomer Homooligomer；Protein × 3 PDB declaration: trimeric	Chain A 292–466（175 aa） Chain B 292–466（175 aa） Chain C 292–466（175 aa）	Not recorded	A1CA9 N-(1,3-thiazol-2-yl)quinoxaline-6-carboxamide × 3	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；pH 6.5；291 K；10-15% PEG 3350, 0.1 M Bis-TRIS pH 6.5	Resolution 2.80 Å R-free 0.295
9OLB Identification of ligands for E3 ligases using fragment-based methods Deposited 2025-05-12	Different construct Different oligomeric state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 1 Protein heterocomplex Heteromer；Protein × 2 PDB declaration: dimeric	Chain A 292–466（175 aa）	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；293 K；10-15% PEG 3350, 0.1 M Bis-TRIS pH 6.5	Resolution 2.62 Å R-free 0.276
9OLB Identification of ligands for E3 ligases using fragment-based methods Deposited 2025-05-12	Different construct Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 2 Protein monomer Monomer；Protein × 1 PDB declaration: monomeric	Chain B 292–466（175 aa）	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；293 K；10-15% PEG 3350, 0.1 M Bis-TRIS pH 6.5	Resolution 2.62 Å R-free 0.276
9OLB Identification of ligands for E3 ligases using fragment-based methods Deposited 2025-05-12	Different construct Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics	Assembly 3 Protein monomer Monomer；Protein × 1 PDB declaration: monomeric	Chain C 292–466（175 aa）	Not recorded	No recorded non-water small molecule	X-RAY DIFFRACTION X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP；293 K；10-15% PEG 3350, 0.1 M Bis-TRIS pH 6.5	Resolution 2.62 Å R-free 0.276

7 other PDB entries and 10 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence

UniProt name	TRAF4_HUMAN
Isoform	—
PDB entities	1
Chains and sequence ranges	Author chain A； PDBConstruct 8–66； UniProt 190–248

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.

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2. Structure Basics 2. Structure Basics

Entry ID entry_id	2eod
Deposition date deposition_date	2007-03-29
Structure title title	Solution structure of TRAF-type zinc finger domains (190- 248) from human TNF receptor-associated factor 4
Keywords keywords	;zinc binding, TNF, TNFR, NF-kB, Structural Genomics, NPPSFA, National Project on Protein Structural and Functional Analyses, RIKEN Structural Genomics/Proteomics Initiative, RSGI, SIGNALING PROTEIN ;; SIGNALING PROTEIN
Experimental Method method	SOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier	16.53 Å
Radius of gyration Rg (electron density) rg_electron	16.79 Å
Forward intensity I(0) i0	359889000.00
Molecular weight molecular_weight	144070.0 kDa
Excluded volume excluded_volume	173510 Å³
Envelope volume envelope_volume	28340 Å³
Hydration-shell volume shell_volume	12043 Å³
Envelope diameter envelope_diameter	78.1 Å
Shell Rg shell_rg	26.58 Å
Envelope Rg envelope_rg	24.21 Å
Shape Rg shape_rg	16.81 Å
Total Rg total_rg	16.94 Å
Total atoms total_atoms	19240
Residues n_residues	1320
Spherical-harmonic order n_harmonics	20
q range q_range	— – 0.5000 Å⁻¹
Data points n_points	101
Shell type shell_type	directional
Solvent electron density solvent_density	0.3340 e/Å³
Shell contrast contrast_shell	0.0300 e/Å³
CRYSOL version crysol_version	4.1.3

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4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax	43.8 Å
Rg (real space) rg_real	14.97 Å
Rg uncertainty (real space) rg_real_error	0.12 Å
I(0) (real space) i0_real	3.4040e+08
I(0) uncertainty (real space) i0_real_error	3.1900e+06
Rg (reciprocal space) rg_reciprocal	17.07 Å
I(0) (reciprocal space) i0_reciprocal	359900000.0000
Solution quality estimate total_estimate	0.6241
Solution quality rating solution_quality	REASONABLE a REASONABLE solution
P(r) peaks n_peaks	1
Primary peak position r_peak_primary	10.8 Å
Skewness Skewness skewness	0.375
Kurtosis Kurtosis kurtosis	-0.782
Angular range angular_range	— – 0.4800 Å⁻¹
Current regularization parameter α current_alpha	2.8860
Highest regularization parameter α highest_alpha	55400.0000
Real-space data points n_real_points	78
GNOM version gnom_version	4.1.3
Quality Criteria quality_criteria	AN1: 0.009; Oscil: 0.909; Stabil: 0.988; Sysdev: 0.000; Positv: 1.000; Valcen: 0.492; Smooth: 0.000

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5. Crystallography and Experiment 5. Crystallography & Experiment

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6. Entities and Polymers Entities & Polymers (2)

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7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

Domain ID domain_id	2eodA00
Class class	3 — Alpha Beta
Architecture architecture	30 — 2-Layer Sandwich
Topology topology	40 — Herpes Virus-1
Homologous superfamily homologous superfamily	10 — Zinc/RING finger domain, C3HC4 (zinc finger)

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8. Citations (1)

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Description description	TNF receptor-associated factor 4
Molecular weight formula_weight	7097.0 kDa
Source method src_method	man
Copy count entity_count	1

Polymer type type	polypeptide(L)
Chain IDs strand_id	A
Atom count atom_count	19240

来源生物 organism	Homo sapiens
通用名 common_name	human
NCBI Class编号 ncbi_taxonomy_id	9606

Description description	ZINC ION
Molecular weight formula_weight	65.4 kDa
Source method src_method	syn
Copy count entity_count	2

fit	/app/data/saxs_computation/eo/2eod/2eod.fit
pddf	/app/data/pr_computation/eo/2eod/2eod.pr.out
profile	/app/data/saxs_computation/eo/2eod/2eod.dat

Solution structure of TRAF-type zinc finger domains (190- 248) from human TNF receptor-associated factor 4

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

TNF receptor-associated factor 4

State in the Current Structure

Other States of the Same Protein in the Database

SAXS scattering curve SAXS Profile

P(r) Distance Distribution P(r) Distribution

2. Structure Basics 2. Structure Basics

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

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

Entity 1 Entity 1 polymer

Polymer Polymer

来源 Source

Entity 2 Entity 2 non-polymer

7. Fold Classification (SCOP + CATH) 1 domains

CATH v4.4 (1 domains)

8. Citations (1)

9. Files and Curves (10)

Files (7)

Curves (3)