6t3y

Improved High Resolution Structure of MHC Class II complex

Method: X-RAY DIFFRACTION Dmax: 78.5 Å Quality: GOOD

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

MHC class II alpha chain

Gallus gallus

UniProt Q4U5Z6

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 27–207 Not recorded MHC class II beta chain 2 × 1 (B5BSA0) GOL GLYCEROL × 3 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.5;293 K;0.2 M Na Acetate 0.1 M TRIS 30 %w/v PEG 4K Resolution 1.70 Å R-free 0.202

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.

4 other PDB entries and 6 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name Q4U5Z6_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–183; UniProt 27–207

MHC class II beta chain 2

Gallus gallus

UniProt B5BSA0

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 30–215 Not recorded MHC class II alpha chain × 1 (Q4U5Z6) GOL GLYCEROL × 3 ACT ACETATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 8.5;293 K;0.2 M Na Acetate 0.1 M TRIS 30 %w/v PEG 4K Resolution 1.70 Å R-free 0.202

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.

1 other PDB entries and 1 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name B5BSA0_CHICK
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 39–224; UniProt 30–215

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 6t3y

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6t3y
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6t3y
Deposition date deposition_date2019-10-11
Structure title titleImproved High Resolution Structure of MHC Class II complex
Keywords keywordsMHC II, Immune Synapse, 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_guinier24.23
Radius of gyration Rg (electron density) rg_electron23.12
Forward intensity I(0) i031750500.00
Molecular weight molecular_weight43100.0 kDa
Excluded volume excluded_volume53692 ų
Envelope volume envelope_volume65132 ų
Hydration-shell volume shell_volume23752 ų
Envelope diameter envelope_diameter83.4
Shell Rg shell_rg29.98
Envelope Rg envelope_rg23.49
Shape Rg shape_rg23.09
Total Rg total_rg24.05
Total atoms total_atoms3076
Residues n_residues379
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 dmax78.5
Rg (real space) rg_real24.23
Rg uncertainty (real space) rg_real_error0.74
I(0) (real space) i0_real3.1750e+07
I(0) uncertainty (real space) i0_real_error4.9120e+05
Rg (reciprocal space) rg_reciprocal24.23
I(0) (reciprocal space) i0_reciprocal31750000.0000
Solution quality estimate total_estimate0.8073
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary27.0
Skewness Skewness skewness0.343
Kurtosis Kurtosis kurtosis-0.363
Angular range angular_range— – 0.3300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha8677000.0000
Real-space data points n_real_points65
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.861; Stabil: 0.975; Sysdev: 1.000; Positv: 1.000; Valcen: 0.983; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd6t3ya1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.19 — MHC antigen-recognition domain
Superfamily Superfamily superfamilyd.19.1 — MHC antigen-recognition domain
Family Family familyd.19.1.0 — automated matches
Domain ID domain_idd6t3ya2
Class classb — All beta proteins
Fold Fold foldb.1 — Immunoglobulin-like beta-sandwich
Superfamily Superfamily superfamilyb.1.1 — Immunoglobulin
Family Family familyb.1.1.0 — automated matches
Domain ID domain_idd6t3ya3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

8. Citations (1)

9. Files and Curves (10)