6lry

Crystal structure of human endothelin ETB receptor in complex with sarafotoxin S6b

Method: X-RAY DIFFRACTION Dmax: 99.8 Å Quality: REASONABLE

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

Endothelin receptor type B,Endolysin,Endothelin receptor type B

Homo sapiens

UniProt A0A097J809

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 2–161 Mutation:R124Y,D154A,K270A,C1052T,C1095A,S342A,I381A,C396A,C400A,C405A Sarafotoxin-B × 1 (P13208) X-RAY DIFFRACTION X-ray crystallization conditions:LIPIDIC CUBIC PHASE;pH 5;293 K;PEG 600, Ammonium sulfate Resolution 3.00 Å R-free 0.304

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.

16 other PDB entries and 20 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A097J809_BPT4
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 242–401; UniProt 2–161

Endothelin receptor type B,Endolysin,Endothelin receptor type B

Homo sapiens

UniProt P24530

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 66–303 Chain A; UniProt 311–407 Mutation:R124Y,D154A,K270A,C1052T,C1095A,S342A,I381A,C396A,C400A,C405A Sarafotoxin-B × 1 (P13208) X-RAY DIFFRACTION X-ray crystallization conditions:LIPIDIC CUBIC PHASE;pH 5;293 K;PEG 600, Ammonium sulfate Resolution 3.00 Å R-free 0.304

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.

12 other PDB entries and 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name EDNRB_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–241; UniProt 66–303 Author chain A; PDBConstruct 402–498; UniProt 311–407

Sarafotoxin-B

OrganismNot specified

UniProt P13208

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 × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 150–170 Not recorded Endothelin receptor type B,Endolysin,Endothelin receptor type B × 1 (P24530,A0A097J809) X-RAY DIFFRACTION X-ray crystallization conditions:LIPIDIC CUBIC PHASE;pH 5;293 K;PEG 600, Ammonium sulfate Resolution 3.00 Å R-free 0.304

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 SRTX_ATREN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–21; UniProt 150–170

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 6lry

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id6lry
Deposition date deposition_date2020-01-16
Structure title titleCrystal structure of human endothelin ETB receptor in complex with sarafotoxin S6b
Keywords keywordsalpha helical, SIGNALING PROTEIN, MEMBRANE PROTEIN; MEMBRANE PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier31.21
Radius of gyration Rg (electron density) rg_electron30.45
Forward intensity I(0) i043751500.00
Molecular weight molecular_weight55225.0 kDa
Excluded volume excluded_volume70604 ų
Envelope volume envelope_volume91325 ų
Hydration-shell volume shell_volume26486 ų
Envelope diameter envelope_diameter105.0
Shell Rg shell_rg35.59
Envelope Rg envelope_rg30.28
Shape Rg shape_rg30.44
Total Rg total_rg31.03
Total atoms total_atoms3881
Residues n_residues489
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 dmax99.8
Rg (real space) rg_real31.43
Rg uncertainty (real space) rg_real_error0.82
I(0) (real space) i0_real4.3750e+07
I(0) uncertainty (real space) i0_real_error7.7740e+05
Rg (reciprocal space) rg_reciprocal31.34
I(0) (reciprocal space) i0_reciprocal43750000.0000
Solution quality estimate total_estimate0.6189
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary97.8
Skewness Skewness skewness0.370
Kurtosis Kurtosis kurtosis-0.699
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10030000.0000
Real-space data points n_real_points52
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.838; Stabil: 1.000; Sysdev: 0.040; Positv: 1.000; Valcen: 0.657; Smooth: 0.752

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)