8vd2

Human TCR ET650-4 in complex with DQ8-InsC8-15-IAPP1

Method: X-RAY DIFFRACTION Dmax: 126.3 Å Quality: GOOD

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

MHC class II HLA-DQ-alpha chain

Homo sapiens

UniProt Q30069

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 1–185 Mutation:I75C MHC class II HLA-DQ-beta-1 × 1 (O19707) Hybrid insulin peptide (HIP; InsC8-15-IAPP23-29 ) × 1 T-CELL-RECEPTOR, TCR ET650-4 alpha × 1 T-CELL-RECEPTOR, TCR ET650-4 beta × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;293.15 K;0.2 M potassium dihydrogen phosphate (KH2PO4), 15% w/v PEG 20,000 with seeding and additive 30 mM MnCl2 Resolution 2.90 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.

12 other PDB entries and 18 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q30069_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–185; UniProt 1–185

MHC class II HLA-DQ-beta-1

Homo sapiens

UniProt O19707

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 MHC class II HLA-DQ-alpha chain × 1 (Q30069) Hybrid insulin peptide (HIP; InsC8-15-IAPP23-29 ) × 1 T-CELL-RECEPTOR, TCR ET650-4 alpha × 1 T-CELL-RECEPTOR, TCR ET650-4 beta × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;293.15 K;0.2 M potassium dihydrogen phosphate (KH2PO4), 15% w/v PEG 20,000 with seeding and additive 30 mM MnCl2 Resolution 2.90 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.

13 other PDB entries and 20 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name O19707_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–192; 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 8vd2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8vd2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8vd2
Deposition date deposition_date2023-12-14
Structure title titleHuman TCR ET650-4 in complex with DQ8-InsC8-15-IAPP1
Keywords keywordsImmune T cell receptor-pMHC II complex, 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_guinier35.84
Radius of gyration Rg (electron density) rg_electron36.22
Forward intensity I(0) i0126516000.00
Molecular weight molecular_weight89421.0 kDa
Excluded volume excluded_volume111300 ų
Envelope volume envelope_volume145170 ų
Hydration-shell volume shell_volume36470 ų
Envelope diameter envelope_diameter135.1
Shell Rg shell_rg38.51
Envelope Rg envelope_rg36.66
Shape Rg shape_rg36.22
Total Rg total_rg36.38
Total atoms total_atoms6312
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 dmax126.3
Rg (real space) rg_real36.32
Rg uncertainty (real space) rg_real_error1.53
I(0) (real space) i0_real1.2650e+08
I(0) uncertainty (real space) i0_real_error2.3000e+06
Rg (reciprocal space) rg_reciprocal36.02
I(0) (reciprocal space) i0_reciprocal126500000.0000
Solution quality estimate total_estimate0.7920
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary31.6
Skewness Skewness skewness0.657
Kurtosis Kurtosis kurtosis-0.089
Angular range angular_range— – 0.2200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha15730000.0000
Real-space data points n_real_points45
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.663; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.626; Smooth: 0.675

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)