8zfb

Cryo-EM structure of the receptor of xtGPR4-Gs complex in pH7.2

Method: ELECTRON MICROSCOPY Dmax: 70.2 Å Quality: GOOD

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

G-protein coupled receptor 4

Xenopus tropicalis

UniProt A0A6I8PUB9

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 monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain R; UniProt 1–353 Not recorded No other associated polymer ELECTRON MICROSCOPY cryo-EM buffer:pH 7.2 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.78 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.

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

View Construct and Data Evidence
UniProt name A0A6I8PUB9_XENTR
Isoform
PDB entities 1
Chains and sequence ranges Author chain R; PDBConstruct 1–353; UniProt 1–353

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 8zfb

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id8zfb
Deposition date deposition_date2024-05-07
Structure title titleCryo-EM structure of the receptor of xtGPR4-Gs complex in pH7.2
Keywords keywordspH7.2, xtGPR4, receptor, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier21.67
Radius of gyration Rg (electron density) rg_electron20.44
Forward intensity I(0) i014513300.00
Molecular weight molecular_weight29591.0 kDa
Excluded volume excluded_volume37524 ų
Envelope volume envelope_volume46314 ų
Hydration-shell volume shell_volume19453 ų
Envelope diameter envelope_diameter72.6
Shell Rg shell_rg26.42
Envelope Rg envelope_rg20.93
Shape Rg shape_rg20.41
Total Rg total_rg21.45
Total atoms total_atoms2088
Residues n_residues286
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 dmax70.2
Rg (real space) rg_real21.72
Rg uncertainty (real space) rg_real_error0.46
I(0) (real space) i0_real1.4510e+07
I(0) uncertainty (real space) i0_real_error1.9570e+05
Rg (reciprocal space) rg_reciprocal21.71
I(0) (reciprocal space) i0_reciprocal14510000.0000
Solution quality estimate total_estimate0.8655
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.1
Skewness Skewness skewness0.395
Kurtosis Kurtosis kurtosis-0.363
Angular range angular_range— – 0.3650 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2531000.0000
Real-space data points n_real_points68
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.870; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.965; Smooth: 0.676

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

8. Citations (1)

9. Files and Curves (10)