6rmj

Crystal structure of human NGR-TNF

Method: X-RAY DIFFRACTION Dmax: 68.0 Å Quality: EXCELLENT

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 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:N-terminal fusion with CNGRCG peptide No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.2;293 K;50 mM MES, 2.8 M magnesium sulfate, 1 M NaCL, 2% isopropanol Resolution 2.65 Å R-free 0.253

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 7–163; UniProt 77–233 Author chain B; PDBConstruct 7–163; UniProt 77–233 Author chain C; PDBConstruct 7–163; 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 6rmj

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6rmj
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6rmj
Deposition date deposition_date2019-05-07
Structure title titleCrystal structure of human NGR-TNF
Keywords keywordsTNF ALPHA, TNFA, Cytokine, Immune system; CYTOKINE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier22.68
Radius of gyration Rg (electron density) rg_electron20.96
Forward intensity I(0) i037628900.00
Molecular weight molecular_weight48416.0 kDa
Excluded volume excluded_volume61096 ų
Envelope volume envelope_volume72039 ų
Hydration-shell volume shell_volume27308 ų
Envelope diameter envelope_diameter70.3
Shell Rg shell_rg28.93
Envelope Rg envelope_rg21.44
Shape Rg shape_rg20.92
Total Rg total_rg22.06
Total atoms total_atoms6830
Residues n_residues436
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 dmax68.0
Rg (real space) rg_real22.52
Rg uncertainty (real space) rg_real_error0.23
I(0) (real space) i0_real3.7630e+07
I(0) uncertainty (real space) i0_real_error4.4030e+05
Rg (reciprocal space) rg_reciprocal22.56
I(0) (reciprocal space) i0_reciprocal37630000.0000
Solution quality estimate total_estimate0.9064
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary29.9
Skewness Skewness skewness0.078
Kurtosis Kurtosis kurtosis-0.511
Angular range angular_range— – 0.3500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16670000.0000
Real-space data points n_real_points67
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.936; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.975; Smooth: 0.997

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_idd6rmja_
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_idd6rmjb_
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_idd6rmjc_
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_id6rmjA00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily40
Domain ID domain_id6rmjB00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily40
Domain ID domain_id6rmjC00
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology120 — Jelly Rolls
Homologous superfamily homologous superfamily40

8. Citations (1)

9. Files and Curves (10)