8vdu

Crystal structure of hybrid insulin peptide (InsC8-15-IAPP74-80) bound to HLA-DQ8

Method: X-RAY DIFFRACTION Dmax: 130.6 Å Quality: EXCELLENT

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 Other combination Heteromer Protein × 12 其他Polymer 1 PDB declaration: dodecameric(12) Consistent with protein copy count Chain A; UniProt 1–184 Chain D; UniProt 1–184 Chain G; UniProt 1–184 Chain J; UniProt 1–184 Not recorded MHC class II HLA-DQ-beta-1 × 4 (O19707) Hybrid insulin peptide (HIP; InsC8-15-IAPP74-80) × 4 beta-D-mannopyranose-(3-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3 PEG DI(HYDROXYETHYL)ETHER × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;293.15 K;0.2 M Monopotassium phosphate, 17% PEG 8K Resolution 3.50 Å R-free 0.246

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 1–184; UniProt 1–184 Author chain D; PDBConstruct 1–184; UniProt 1–184 Author chain G; PDBConstruct 1–184; UniProt 1–184 Author chain J; PDBConstruct 1–184; UniProt 1–184

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 Other combination Heteromer Protein × 12 其他Polymer 1 PDB declaration: dodecameric(12) Consistent with protein copy count Chain B; UniProt 1–192 Chain E; UniProt 1–192 Chain H; UniProt 1–192 Chain K; UniProt 1–192 Not recorded MHC class II HLA-DQ-alpha chain × 4 (Q30069) Hybrid insulin peptide (HIP; InsC8-15-IAPP74-80) × 4 beta-D-mannopyranose-(3-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 3 PEG DI(HYDROXYETHYL)ETHER × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;293.15 K;0.2 M Monopotassium phosphate, 17% PEG 8K Resolution 3.50 Å R-free 0.246

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 Author chain E; PDBConstruct 1–192; UniProt 1–192 Author chain H; PDBConstruct 1–192; UniProt 1–192 Author chain K; 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 8vdu

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8vdu
Deposition date deposition_date2023-12-17
Structure title titleCrystal structure of hybrid insulin peptide (InsC8-15-IAPP74-80) bound to HLA-DQ8
Keywords keywordspMHC 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_guinier40.85
Radius of gyration Rg (electron density) rg_electron40.33
Forward intensity I(0) i0443261000.00
Molecular weight molecular_weight172400.0 kDa
Excluded volume excluded_volume215480 ų
Envelope volume envelope_volume296010 ų
Hydration-shell volume shell_volume61022 ų
Envelope diameter envelope_diameter127.8
Shell Rg shell_rg46.13
Envelope Rg envelope_rg39.34
Shape Rg shape_rg40.33
Total Rg total_rg40.65
Total atoms total_atoms12191
Residues n_residues1522
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 dmax130.6
Rg (real space) rg_real40.72
Rg uncertainty (real space) rg_real_error1.03
I(0) (real space) i0_real4.4330e+08
I(0) uncertainty (real space) i0_real_error7.0240e+06
Rg (reciprocal space) rg_reciprocal40.85
I(0) (reciprocal space) i0_reciprocal443300000.0000
Solution quality estimate total_estimate0.9059
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary50.2
Skewness Skewness skewness0.149
Kurtosis Kurtosis kurtosis-0.578
Angular range angular_range— – 0.1950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha36760000.0000
Real-space data points n_real_points40
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.940; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.953

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)