8wry

Cryo-EM Structure of Mouse TLR4/MD-2/DLAM3 Complex

Method: ELECTRON MICROSCOPY Dmax: 141.4 Å Quality: GOOD

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

Lymphocyte antigen 96

Mus musculus

UniProt Q9JHF9

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 × 4 其他Polymer 6 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 19–160 Chain D; UniProt 19–160 Not recorded Toll-like receptor 4 × 2 (Q9QUK6) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 6 2IL (3R)-3-(dodecanoyloxy)tetradecanoic acid × 4 0IL (3R)-3-(tetradecanoyloxy)tetradecanoic acid × 2 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 16 GP4 2-amino-2-deoxy-4-O-phosphono-alpha-D-glucopyranose × 2 XIQ 2-(hydroxymethyl)-5-methoxy-3,6-bis(oxidanyl)pyran-4-one × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.60 Å

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.

9 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LY96_MOUSE
Isoform
PDB entities 1
Chains and sequence ranges Author chain C; PDBConstruct 1–142; UniProt 19–160 Author chain D; PDBConstruct 1–142; UniProt 19–160

Toll-like receptor 4

Mus musculus

UniProt Q9QUK6

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 × 4 其他Polymer 6 PDB declaration: tetrameric(4) Consistent with protein copy count Chain A; UniProt 26–629 Chain B; UniProt 26–629 Not recorded Lymphocyte antigen 96 × 2 (Q9JHF9) 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose × 6 2IL (3R)-3-(dodecanoyloxy)tetradecanoic acid × 4 0IL (3R)-3-(tetradecanoyloxy)tetradecanoic acid × 2 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 16 GP4 2-amino-2-deoxy-4-O-phosphono-alpha-D-glucopyranose × 2 XIQ 2-(hydroxymethyl)-5-methoxy-3,6-bis(oxidanyl)pyran-4-one × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.60 Å

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.

9 other PDB entries and 14 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name TLR4_MOUSE
Isoform
PDB entities 2
Chains and sequence ranges Author chain A; PDBConstruct 1–604; UniProt 26–629 Author chain B; PDBConstruct 1–604; UniProt 26–629

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 8wry

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8wry
Deposition date deposition_date2023-10-16
Structure title titleCryo-EM Structure of Mouse TLR4/MD-2/DLAM3 Complex
Keywords keywordsInnate immune system, Toll-like receptors, TLR4 agonist, Vaccine adjuvants, Disaccharide-based Lipid A Mimetics, IMMUNE SYSTEM; IMMUNE SYSTEM
Experimental Method methodELECTRON MICROSCOPY

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier41.72
Radius of gyration Rg (electron density) rg_electron41.41
Forward intensity I(0) i0862397000.00
Molecular weight molecular_weight162820.0 kDa
Excluded volume excluded_volume158890 ų
Envelope volume envelope_volume310300 ų
Hydration-shell volume shell_volume63130 ų
Envelope diameter envelope_diameter147.2
Shell Rg shell_rg46.26
Envelope Rg envelope_rg40.74
Shape Rg shape_rg41.41
Total Rg total_rg41.61
Total atoms total_atoms12324
Residues n_residues1462
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 dmax141.4
Rg (real space) rg_real41.71
Rg uncertainty (real space) rg_real_error1.57
I(0) (real space) i0_real8.6240e+08
I(0) uncertainty (real space) i0_real_error1.6810e+07
Rg (reciprocal space) rg_reciprocal41.72
I(0) (reciprocal space) i0_reciprocal862400000.0000
Solution quality estimate total_estimate0.8591
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary52.1
Skewness Skewness skewness0.369
Kurtosis Kurtosis kurtosis-0.146
Angular range angular_range— – 0.1900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha39780000.0000
Real-space data points n_real_points39
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.782; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.819

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (8)

8. Citations (1)

9. Files and Curves (10)