8yx9

CD40 in complex with Dacetuzumab Fab

Method: X-RAY DIFFRACTION Dmax: 227.3 Å Quality: GOOD

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

Tumor necrosis factor receptor superfamily member 5

Homo sapiens

UniProt P25942

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 21–193 Not recorded Dacetuzumab, Heavy chain × 1 Dacetuzumab, light chain × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293.15 K;0.2 M Ammonium citrate tribasic pH 7.0 20% w/v Polyethylene glycol 3,350 Resolution 2.80 Å R-free 0.262
2 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain J; UniProt 21–193 Not recorded Dacetuzumab, Heavy chain × 1 Dacetuzumab, light chain × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293.15 K;0.2 M Ammonium citrate tribasic pH 7.0 20% w/v Polyethylene glycol 3,350 Resolution 2.80 Å R-free 0.262
3 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain D; UniProt 21–193 Not recorded Dacetuzumab, Heavy chain × 1 Dacetuzumab, light chain × 1 GOL GLYCEROL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293.15 K;0.2 M Ammonium citrate tribasic pH 7.0 20% w/v Polyethylene glycol 3,350 Resolution 2.80 Å R-free 0.262
4 Protein heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain K; UniProt 21–193 Not recorded Dacetuzumab, Heavy chain × 1 Dacetuzumab, light chain × 1 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;293.15 K;0.2 M Ammonium citrate tribasic pH 7.0 20% w/v Polyethylene glycol 3,350 Resolution 2.80 Å R-free 0.262

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.

13 other PDB entries and 31 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TNR5_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain A; PDBConstruct 1–173; UniProt 21–193 Author chain D; PDBConstruct 1–173; UniProt 21–193 Author chain J; PDBConstruct 1–173; UniProt 21–193 Author chain K; PDBConstruct 1–173; UniProt 21–193

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 8yx9

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8yx9
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8yx9
Deposition date deposition_date2024-04-02
Structure title titleCD40 in complex with Dacetuzumab Fab
Keywords keywordsCD40, Dacetuzumab, Bleselumab, agonist activity, tumor necrosis factor, IMMUNE SYSTEM; IMMUNE SYSTEM
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier60.43
Radius of gyration Rg (electron density) rg_electron61.80
Forward intensity I(0) i0889391000.00
Molecular weight molecular_weight239390.0 kDa
Excluded volume excluded_volume296330 ų
Envelope volume envelope_volume494360 ų
Hydration-shell volume shell_volume77635 ų
Envelope diameter envelope_diameter308.2
Shell Rg shell_rg51.18
Envelope Rg envelope_rg65.92
Shape Rg shape_rg61.71
Total Rg total_rg61.74
Total atoms total_atoms16810
Residues n_residues2199
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 dmax227.3
Rg (real space) rg_real61.17
Rg uncertainty (real space) rg_real_error2.79
I(0) (real space) i0_real8.8660e+08
I(0) uncertainty (real space) i0_real_error1.8940e+07
Rg (reciprocal space) rg_reciprocal59.06
I(0) (reciprocal space) i0_reciprocal885000000.0000
Solution quality estimate total_estimate0.7779
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary61.2
Skewness Skewness skewness0.904
Kurtosis Kurtosis kurtosis0.601
Angular range angular_range— – 0.1300 −1
Current regularization parameter α current_alpha0.0154
Highest regularization parameter α highest_alpha42290000.0000
Real-space data points n_real_points27
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.001; Oscil: 0.426; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.933; Smooth: 0.893

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)