9ejg

Peptide-independent T cell receptor recognition of HLA-DQ2

Method: X-RAY DIFFRACTION Dmax: 119.6 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 glia-omega 1 peptide × 1 G9 T cell receptor alpha chain × 1 G9 T cell receptor beta chain × 1 MHC class II HLA-DQ-beta-1 × 1 (O19712) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 FMT FORMIC ACID × 5 GOL GLYCEROL × 2 ACT ACETATE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;8% Tacsimate, pH 8.0, 20-24% w/v PEG3350 Resolution 2.20 Å R-free 0.225

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 1–194 Not recorded HLA class II histocompatibility antigen, DQ alpha 1 chain × 1 (P01909) glia-omega 1 peptide × 1 G9 T cell receptor alpha chain × 1 G9 T cell receptor beta chain × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 FMT FORMIC ACID × 5 GOL GLYCEROL × 2 ACT ACETATE ION × 3 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;8% Tacsimate, pH 8.0, 20-24% w/v PEG3350 Resolution 2.20 Å R-free 0.225

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 5
Chains and sequence ranges Author chain B; PDBConstruct 1–194; UniProt 1–194

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 9ejg

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9ejg
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9ejg
Deposition date deposition_date2024-11-27
Structure title titlePeptide-independent T cell receptor recognition of HLA-DQ2
Keywords keywordsT cell receptor, immune receptor, human leukocyte antigen, 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_guinier37.05
Radius of gyration Rg (electron density) rg_electron37.21
Forward intensity I(0) i0127323000.00
Molecular weight molecular_weight90093.0 kDa
Excluded volume excluded_volume112220 ų
Envelope volume envelope_volume150670 ų
Hydration-shell volume shell_volume36316 ų
Envelope diameter envelope_diameter128.6
Shell Rg shell_rg40.14
Envelope Rg envelope_rg36.88
Shape Rg shape_rg37.23
Total Rg total_rg37.33
Total atoms total_atoms6362
Residues n_residues813
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 dmax119.6
Rg (real space) rg_real37.42
Rg uncertainty (real space) rg_real_error1.34
I(0) (real space) i0_real1.2730e+08
I(0) uncertainty (real space) i0_real_error2.2640e+06
Rg (reciprocal space) rg_reciprocal37.19
I(0) (reciprocal space) i0_reciprocal127300000.0000
Solution quality estimate total_estimate0.8174
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary36.1
Skewness Skewness skewness0.498
Kurtosis Kurtosis kurtosis-0.465
Angular range angular_range— – 0.2150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10920000.0000
Real-space data points n_real_points44
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.868; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.752; Smooth: 0.266

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (10)

8. Citations (1)

9. Files and Curves (10)