7sg2

XPA5 TCR in complex with HLA-DQ2-omega1

Method: X-RAY DIFFRACTION Dmax: 185.9 Å Quality: REASONABLE

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) T-cell receptor, xpa5, alpha chain × 1 T-cell receptor, xpa5, beta chain × 1 DQ2-glia-omega1 peptide × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 EDO 1,2-ETHANEDIOL × 1 ACT ACETATE ION × 1 CA CALCIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;Mother liquor: 16-18% PEG3350, 0.12-0.14 M CaOAc, 0.1 M Tris/HCl at pH 8.0, Additives: 2 mM reduced and oxidised Glutathione Resolution 3.10 Å R-free 0.259
2 Protein heterocomplex Heteromer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain F; UniProt 24–206 Not recorded MHC class II HLA-DQ-beta-1 × 1 (O19712) T-cell receptor, xpa5, alpha chain × 1 T-cell receptor, xpa5, beta chain × 1 DQ2-glia-omega1 peptide × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 EDO 1,2-ETHANEDIOL × 2 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;Mother liquor: 16-18% PEG3350, 0.12-0.14 M CaOAc, 0.1 M Tris/HCl at pH 8.0, Additives: 2 mM reduced and oxidised Glutathione Resolution 3.10 Å R-free 0.259

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 35 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 Author chain F; 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) T-cell receptor, xpa5, alpha chain × 1 T-cell receptor, xpa5, beta chain × 1 DQ2-glia-omega1 peptide × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 EDO 1,2-ETHANEDIOL × 1 ACT ACETATE ION × 1 CA CALCIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;Mother liquor: 16-18% PEG3350, 0.12-0.14 M CaOAc, 0.1 M Tris/HCl at pH 8.0, Additives: 2 mM reduced and oxidised Glutathione Resolution 3.10 Å R-free 0.259
2 Protein heterocomplex Heteromer Protein × 5 PDB declaration: pentameric(5) Consistent with protein copy count Chain G; UniProt 1–192 Not recorded HLA class II histocompatibility antigen, DQ alpha 1 chain × 1 (P01909) T-cell receptor, xpa5, alpha chain × 1 T-cell receptor, xpa5, beta chain × 1 DQ2-glia-omega1 peptide × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 EDO 1,2-ETHANEDIOL × 2 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293.15 K;Mother liquor: 16-18% PEG3350, 0.12-0.14 M CaOAc, 0.1 M Tris/HCl at pH 8.0, Additives: 2 mM reduced and oxidised Glutathione Resolution 3.10 Å R-free 0.259

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 26 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 14–205; UniProt 1–192 Author chain G; PDBConstruct 14–205; 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 7sg2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7sg2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7sg2
Deposition date deposition_date2021-10-04
Structure title titleXPA5 TCR in complex with HLA-DQ2-omega1
Keywords keywordsTCR-pHLA, 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_guinier51.64
Radius of gyration Rg (electron density) rg_electron52.22
Forward intensity I(0) i0476072000.00
Molecular weight molecular_weight177980.0 kDa
Excluded volume excluded_volume221900 ų
Envelope volume envelope_volume324210 ų
Hydration-shell volume shell_volume58685 ų
Envelope diameter envelope_diameter193.9
Shell Rg shell_rg46.13
Envelope Rg envelope_rg53.20
Shape Rg shape_rg52.21
Total Rg total_rg51.98
Total atoms total_atoms12544
Residues n_residues1567
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 dmax185.9
Rg (real space) rg_real52.40
Rg uncertainty (real space) rg_real_error2.43
I(0) (real space) i0_real4.7610e+08
I(0) uncertainty (real space) i0_real_error9.0870e+06
Rg (reciprocal space) rg_reciprocal51.02
I(0) (reciprocal space) i0_reciprocal475200000.0000
Solution quality estimate total_estimate0.5139
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary43.4
Skewness Skewness skewness0.772
Kurtosis Kurtosis kurtosis0.128
Angular range angular_range— – 0.1500 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha31250000.0000
Real-space data points n_real_points31
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.558; Stabil: 1.000; Sysdev: 0.007; Positv: 1.000; Valcen: 0.771; Smooth: 0.208

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (10)

8. Citations (1)

9. Files and Curves (10)