7sg0

W316 TCR in complex with HLA-DQ2-omega1

Method: X-RAY DIFFRACTION Dmax: 134.1 Å Quality: GOOD

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

HLA class II histocompatibility antigen, DQ alpha 1 chain

Homo sapiens

UniProt P01909

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain A; UniProt 24–206 Not recorded MHC class II HLA-DQ-beta-1 × 1 (O19712) DQ2-glia-omega1 peptide × 1 T-cell receptor, w316, alpha chain × 1 T-cell receptor, w316, beta chain × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 EDO 1,2-ETHANEDIOL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;24% PEG3350, 0.25 M (NH4)2SO4 and 0.1 M Tris/HCl at pH 8.0 Resolution 3.00 Å R-free 0.230

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.

21 other PDB entries and 36 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DQA1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–183; UniProt 24–206

MHC class II HLA-DQ-beta-1

Homo sapiens

UniProt O19712

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 × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain B; UniProt 1–192 Not recorded HLA class II histocompatibility antigen, DQ alpha 1 chain × 1 (P01909) DQ2-glia-omega1 peptide × 1 T-cell receptor, w316, alpha chain × 1 T-cell receptor, w316, beta chain × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 EDO 1,2-ETHANEDIOL × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;24% PEG3350, 0.25 M (NH4)2SO4 and 0.1 M Tris/HCl at pH 8.0 Resolution 3.00 Å R-free 0.230

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.

16 other PDB entries and 27 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name O19712_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 16–207; UniProt 1–192

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 7sg0

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7sg0
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7sg0
Deposition date deposition_date2021-10-04
Structure title titleW316 TCR in complex with HLA-DQ2-omega1
Keywords keywordsTCR-pHLA complex, Celiac disease, 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_guinier37.14
Radius of gyration Rg (electron density) rg_electron37.45
Forward intensity I(0) i0130563000.00
Molecular weight molecular_weight91334.0 kDa
Excluded volume excluded_volume113900 ų
Envelope volume envelope_volume155400 ų
Hydration-shell volume shell_volume37608 ų
Envelope diameter envelope_diameter138.1
Shell Rg shell_rg39.45
Envelope Rg envelope_rg37.92
Shape Rg shape_rg37.42
Total Rg total_rg37.68
Total atoms total_atoms6446
Residues n_residues804
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 dmax134.1
Rg (real space) rg_real37.70
Rg uncertainty (real space) rg_real_error1.52
I(0) (real space) i0_real1.3060e+08
I(0) uncertainty (real space) i0_real_error2.3900e+06
Rg (reciprocal space) rg_reciprocal37.36
I(0) (reciprocal space) i0_reciprocal130500000.0000
Solution quality estimate total_estimate0.7698
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary34.3
Skewness Skewness skewness0.654
Kurtosis Kurtosis kurtosis-0.118
Angular range angular_range— – 0.2150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha16530000.0000
Real-space data points n_real_points44
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.605; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.473; Smooth: 0.714

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)