8w84

HLA-DQ2.5-alpha2 gliadin peptide in complex with DQN0344AE02

Method: X-RAY DIFFRACTION Dmax: 136.0 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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 24–206 Mutation:C47S DQN0344AE02 Fab heavy chain × 1 DQN0344AE02 Fab light chain × 1 MHC class II HLA-DQ-beta-1 - alpha2 gliadin peptide chimeric protein × 1 (O19712) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4;293 K;80 mM di-Sodium malonate (pH4.0), 9.6 %w/v Polyethylene glycol 3,350, and 25 %v/v Ethylene glycol as cryoprotectant Resolution 2.10 Å R-free 0.325

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 3
Chains and sequence ranges Author chain C; PDBConstruct 1–183; UniProt 24–206

MHC class II HLA-DQ-beta-1 - alpha2 gliadin peptide chimeric protein

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 × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain D; UniProt 1–190 Not recorded DQN0344AE02 Fab heavy chain × 1 DQN0344AE02 Fab light chain × 1 HLA class II histocompatibility antigen, DQ alpha 1 chain × 1 (P01909) NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 4;293 K;80 mM di-Sodium malonate (pH4.0), 9.6 %w/v Polyethylene glycol 3,350, and 25 %v/v Ethylene glycol as cryoprotectant Resolution 2.10 Å R-free 0.325

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 4
Chains and sequence ranges Author chain D; PDBConstruct 31–220; UniProt 1–190

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 8w84

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8w84
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8w84
Deposition date deposition_date2023-08-31
Structure title titleHLA-DQ2.5-alpha2 gliadin peptide in complex with DQN0344AE02
Keywords keywordsCELIAC DISEASE, ANTIBODY, 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_guinier36.80
Radius of gyration Rg (electron density) rg_electron37.16
Forward intensity I(0) i0122299000.00
Molecular weight molecular_weight88466.0 kDa
Excluded volume excluded_volume110370 ų
Envelope volume envelope_volume147780 ų
Hydration-shell volume shell_volume36381 ų
Envelope diameter envelope_diameter143.5
Shell Rg shell_rg38.58
Envelope Rg envelope_rg38.13
Shape Rg shape_rg37.14
Total Rg total_rg37.36
Total atoms total_atoms6248
Residues n_residues812
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 dmax136.0
Rg (real space) rg_real37.41
Rg uncertainty (real space) rg_real_error1.78
I(0) (real space) i0_real1.2230e+08
I(0) uncertainty (real space) i0_real_error2.5470e+06
Rg (reciprocal space) rg_reciprocal37.03
I(0) (reciprocal space) i0_reciprocal122300000.0000
Solution quality estimate total_estimate0.7537
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary34.8
Skewness Skewness skewness0.698
Kurtosis Kurtosis kurtosis-0.024
Angular range angular_range— – 0.2150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha13310000.0000
Real-space data points n_real_points44
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.524; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.381; Smooth: 0.841

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (6)

8. Citations (1)

9. Files and Curves (10)