9uok

Structure of the complex of LGR4_ECD with Norrin

Method: ELECTRON MICROSCOPY Dmax: 118.8 Å Quality: GOOD

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

Leucine-rich repeat-containing G-protein coupled receptor 4

Homo sapiens

UniProt Q9BXB1

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain C; UniProt 24–951 Not recorded MB52 × 1 Norrin,Immunoglobulin gamma-1 heavy chain × 2 (Q00604,P0DOX5) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.05 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.

22 other PDB entries and 23 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name LGR4_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 16–943; UniProt 24–951

Norrin,Immunoglobulin gamma-1 heavy chain

Homo sapiens

UniProt P0DOX5

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain E; UniProt 220–449 Chain F; UniProt 220–449 Not recorded MB52 × 1 Leucine-rich repeat-containing G-protein coupled receptor 4 × 1 (Q9BXB1) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.05 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.

105 other PDB entries and 128 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name IGG1_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain E; PDBConstruct 172–401; UniProt 220–449 Author chain F; PDBConstruct 172–401; UniProt 220–449

Norrin,Immunoglobulin gamma-1 heavy chain

Homo sapiens

UniProt Q00604

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Insufficient information Heteromer Protein × 4 PDB declaration: tetrameric(4) Consistent with protein copy count Chain E; UniProt 25–133 Chain F; UniProt 25–133 Not recorded MB52 × 1 Leucine-rich repeat-containing G-protein coupled receptor 4 × 1 (Q9BXB1) ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.05 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.

11 other PDB entries and 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name NDP_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain E; PDBConstruct 39–147; UniProt 25–133 Author chain F; PDBConstruct 39–147; UniProt 25–133

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 9uok

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9uok
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9uok
Deposition date deposition_date2025-04-25
Structure title titleStructure of the complex of LGR4_ECD with Norrin
Keywords keywordsLGR4 Norrin, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier35.97
Radius of gyration Rg (electron density) rg_electron36.01
Forward intensity I(0) i0114091000.00
Molecular weight molecular_weight83534.0 kDa
Excluded volume excluded_volume103850 ų
Envelope volume envelope_volume142320 ų
Hydration-shell volume shell_volume35730 ų
Envelope diameter envelope_diameter127.1
Shell Rg shell_rg38.66
Envelope Rg envelope_rg36.07
Shape Rg shape_rg35.99
Total Rg total_rg36.26
Total atoms total_atoms5851
Residues n_residues752
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 dmax118.8
Rg (real space) rg_real36.10
Rg uncertainty (real space) rg_real_error1.23
I(0) (real space) i0_real1.1410e+08
I(0) uncertainty (real space) i0_real_error2.2360e+06
Rg (reciprocal space) rg_reciprocal36.03
I(0) (reciprocal space) i0_reciprocal114100000.0000
Solution quality estimate total_estimate0.8824
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary40.5
Skewness Skewness skewness0.341
Kurtosis Kurtosis kurtosis-0.505
Angular range angular_range— – 0.2200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha9562000.0000
Real-space data points n_real_points45
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.923; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.891; Smooth: 0.807

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)