7sus

Crystal structure of Apelin receptor in complex with small molecule

Method: X-RAY DIFFRACTION Dmax: 90.8 Å Quality: GOOD

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

Apelin receptor, with Rubredoxin insertion

Homo sapiens

UniProt P00268

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 Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1–54 Mutation:V117A,E174C,T177N,M217C,I250C,C325L,C326M ZN ZINC ION × 1 8EH (1R,2S)-N-[4-(2,6-dimethoxyphenyl)-5-(6-methylpyridin-2-yl)-1,2,4-triazol-3-yl]-1-(5-methylpyrimidin-2-yl)-1-oxidanyl-propane-2-sulfonamide × 1 OLC (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate × 1 X-RAY DIFFRACTION X-ray crystallization conditions:LIPIDIC CUBIC PHASE;293 K;100 mM MES pH 6.1, 26% PEG500 DME, 125 mM MgCl2, 100 mM NaCl Resolution 2.70 Å R-free 0.274

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.

44 other PDB entries and 58 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name RUBR_CLOPA
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 248–301; UniProt 1–54

Apelin receptor, with Rubredoxin insertion

Homo sapiens

UniProt P35414

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 Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 7–229 Chain A; UniProt 243–330 Mutation:V117A,E174C,T177N,M217C,I250C,C325L,C326M ZN ZINC ION × 1 8EH (1R,2S)-N-[4-(2,6-dimethoxyphenyl)-5-(6-methylpyridin-2-yl)-1,2,4-triazol-3-yl]-1-(5-methylpyrimidin-2-yl)-1-oxidanyl-propane-2-sulfonamide × 1 OLC (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate × 1 X-RAY DIFFRACTION X-ray crystallization conditions:LIPIDIC CUBIC PHASE;293 K;100 mM MES pH 6.1, 26% PEG500 DME, 125 mM MgCl2, 100 mM NaCl Resolution 2.70 Å R-free 0.274

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.

33 other PDB entries and 33 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name APJ_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 25–247; UniProt 7–229 Author chain A; PDBConstruct 302–389; UniProt 243–330

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 7sus

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 7sus
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2. Structure Basics 2. Structure Basics

Entry ID entry_id7sus
Deposition date deposition_date2021-11-18
Structure title titleCrystal structure of Apelin receptor in complex with small molecule
Keywords keywordsGPCR, Class A GPCR, small molecule, MEMBRANE PROTEIN, Apelin receptor; MEMBRANE PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier26.71
Radius of gyration Rg (electron density) rg_electron25.73
Forward intensity I(0) i023519400.00
Molecular weight molecular_weight38976.0 kDa
Excluded volume excluded_volume49447 ų
Envelope volume envelope_volume63481 ų
Hydration-shell volume shell_volume22484 ų
Envelope diameter envelope_diameter92.3
Shell Rg shell_rg30.43
Envelope Rg envelope_rg26.25
Shape Rg shape_rg25.72
Total Rg total_rg26.39
Total atoms total_atoms2737
Residues n_residues347
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 dmax90.8
Rg (real space) rg_real26.95
Rg uncertainty (real space) rg_real_error0.80
I(0) (real space) i0_real2.3520e+07
I(0) uncertainty (real space) i0_real_error3.5980e+05
Rg (reciprocal space) rg_reciprocal26.88
I(0) (reciprocal space) i0_reciprocal23520000.0000
Solution quality estimate total_estimate0.8421
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.6
Skewness Skewness skewness0.495
Kurtosis Kurtosis kurtosis-0.366
Angular range angular_range— – 0.2950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3242000.0000
Real-space data points n_real_points60
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.803; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.664; Smooth: 0.871

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)