1a8m

TUMOR NECROSIS FACTOR ALPHA, R31D MUTANT

Method: X-RAY DIFFRACTION Dmax: 73.1 Å Quality: GOOD

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

TUMOR NECROSIS FACTOR ALPHA

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 homooligomer Homooligomer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 77–233 Chain B; UniProt 77–233 Chain C; UniProt 77–233 Mutation:R31D No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:pH 5.5;CRYSTALLIZED FROM 88% MGSO4, 1-2% PEG 400, 0.2 M MES, PH 5.5. Resolution 2.30 Å R-free 0.240

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 1–157; UniProt 77–233 Author chain B; PDBConstruct 1–157; UniProt 77–233 Author chain C; PDBConstruct 1–157; UniProt 77–233

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 1a8m

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1a8m
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1a8m
Deposition date deposition_date1998-03-27
Structure title titleTUMOR NECROSIS FACTOR ALPHA, R31D MUTANT
Keywords keywordsLYMPHOKINE, CYTOKINE, CYTOTOXIN; LYMPHOKINE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.90
Radius of gyration Rg (electron density) rg_electron21.19
Forward intensity I(0) i041100600.00
Molecular weight molecular_weight50376.0 kDa
Excluded volume excluded_volume63390 ų
Envelope volume envelope_volume72863 ų
Hydration-shell volume shell_volume27512 ų
Envelope diameter envelope_diameter74.7
Shell Rg shell_rg29.17
Envelope Rg envelope_rg21.53
Shape Rg shape_rg21.16
Total Rg total_rg22.25
Total atoms total_atoms3561
Residues n_residues456
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 dmax73.1
Rg (real space) rg_real22.73
Rg uncertainty (real space) rg_real_error0.31
I(0) (real space) i0_real4.1100e+07
I(0) uncertainty (real space) i0_real_error5.3610e+05
Rg (reciprocal space) rg_reciprocal22.77
I(0) (reciprocal space) i0_reciprocal41100000.0000
Solution quality estimate total_estimate0.8891
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.4
Skewness Skewness skewness0.087
Kurtosis Kurtosis kurtosis-0.482
Angular range angular_range— – 0.3450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16090000.0000
Real-space data points n_real_points66
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.856; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.986; Smooth: 1.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1a8ma_
Class classb — All beta proteins
Fold Fold foldb.22 — TNF-like
Superfamily Superfamily superfamilyb.22.1 — TNF-like
Family Family familyb.22.1.1 — TNF-like
Domain ID domain_idd1a8mb_
Class classb — All beta proteins
Fold Fold foldb.22 — TNF-like
Superfamily Superfamily superfamilyb.22.1 — TNF-like
Family Family familyb.22.1.1 — TNF-like
Domain ID domain_idd1a8mc_
Class classb — All beta proteins
Fold Fold foldb.22 — TNF-like
Superfamily Superfamily superfamilyb.22.1 — TNF-like
Family Family familyb.22.1.1 — TNF-like

CATH v4.4 (3 domains)

Domain ID domain_id1a8mA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily40
Domain ID domain_id1a8mB00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily40
Domain ID domain_id1a8mC00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily40

8. Citations (2)

9. Files and Curves (10)