8eq6

PD1 signaling receptor bound to FAB Complex

Method: X-RAY DIFFRACTION Dmax: 95.4 Å Quality: GOOD

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

Programmed cell death protein 1

Homo sapiens

UniProt Q15116

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 25–148 Not recorded Antibody FAB light chain × 1 Antibody FAB heavy chain × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 5.5;293 K;20.5% PEG 3350, 0.4M MgCl2, 0.1M Bis-Tris pH 5.5 Resolution 1.65 Å R-free 0.257

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.

33 other PDB entries and 56 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PDCD1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 6–129; UniProt 25–148

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 8eq6

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8eq6
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8eq6
Deposition date deposition_date2022-10-07
Structure title titlePD1 signaling receptor bound to FAB Complex
Keywords keywordsImmune signaling receptor FAB complex, SIGNALING PROTEIN-Immune System complex; SIGNALING PROTEIN/Immune System
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier27.87
Radius of gyration Rg (electron density) rg_electron27.49
Forward intensity I(0) i050175600.00
Molecular weight molecular_weight55020.0 kDa
Excluded volume excluded_volume68649 ų
Envelope volume envelope_volume86496 ų
Hydration-shell volume shell_volume27638 ų
Envelope diameter envelope_diameter102.1
Shell Rg shell_rg33.29
Envelope Rg envelope_rg27.50
Shape Rg shape_rg27.46
Total Rg total_rg28.17
Total atoms total_atoms3877
Residues n_residues503
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 dmax95.4
Rg (real space) rg_real28.06
Rg uncertainty (real space) rg_real_error0.86
I(0) (real space) i0_real5.0180e+07
I(0) uncertainty (real space) i0_real_error7.7440e+05
Rg (reciprocal space) rg_reciprocal28.00
I(0) (reciprocal space) i0_reciprocal50170000.0000
Solution quality estimate total_estimate0.8629
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.1
Skewness Skewness skewness0.517
Kurtosis Kurtosis kurtosis-0.159
Angular range angular_range— – 0.2850 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8253000.0000
Real-space data points n_real_points58
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.814; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.888; Smooth: 0.884

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

8. Citations (1)

9. Files and Curves (10)