6vrh

Cryo-EM structure of the wild-type human serotonin transporter complexed with paroxetine and 8B6 Fab

Method: ELECTRON MICROSCOPY Dmax: 104.2 Å Quality: GOOD

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

Sodium-dependent serotonin transporter

Homo sapiens

UniProt P31645

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 heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–630 Not recorded 8B6 antibody, light chain × 1 (A0A0U5BC76) 8B6 antibody, heavy chain × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 8PR Paroxetine × 1 CL CHLORIDE ION × 1 LMT DODECYL-BETA-D-MALTOSIDE × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.30 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.

29 other PDB entries and 29 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SC6A4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–630; UniProt 1–630

8B6 antibody, light chain

Mus musculus

UniProt A0A0U5BC76

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 heterocomplex Heteromer Protein × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain C; UniProt 117–234 Not recorded Sodium-dependent serotonin transporter × 1 (P31645) 8B6 antibody, heavy chain × 1 NAG 2-acetamido-2-deoxy-beta-D-glucopyranose × 2 8PR Paroxetine × 1 CL CHLORIDE ION × 1 LMT DODECYL-BETA-D-MALTOSIDE × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 8 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.30 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 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name A0A0U5BC76_MOUSE
Isoform
PDB entities 2
Chains and sequence ranges Author chain C; PDBConstruct 97–214; UniProt 117–234

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 6vrh

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id6vrh
Deposition date deposition_date2020-02-07
Structure title titleCryo-EM structure of the wild-type human serotonin transporter complexed with paroxetine and 8B6 Fab
Keywords keywordsantidepressant, complex, transporter, antibody, TRANSPORT PROTEIN; TRANSPORT PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier30.96
Radius of gyration Rg (electron density) rg_electron30.35
Forward intensity I(0) i0103087000.00
Molecular weight molecular_weight86927.0 kDa
Excluded volume excluded_volume111120 ų
Envelope volume envelope_volume133870 ų
Hydration-shell volume shell_volume37642 ų
Envelope diameter envelope_diameter110.1
Shell Rg shell_rg36.90
Envelope Rg envelope_rg30.55
Shape Rg shape_rg30.32
Total Rg total_rg31.04
Total atoms total_atoms6142
Residues n_residues764
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 dmax104.2
Rg (real space) rg_real31.10
Rg uncertainty (real space) rg_real_error0.92
I(0) (real space) i0_real1.0310e+08
I(0) uncertainty (real space) i0_real_error1.6550e+06
Rg (reciprocal space) rg_reciprocal31.04
I(0) (reciprocal space) i0_reciprocal103100000.0000
Solution quality estimate total_estimate0.8621
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary32.7
Skewness Skewness skewness0.481
Kurtosis Kurtosis kurtosis-0.302
Angular range angular_range— – 0.2550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha17610000.0000
Real-space data points n_real_points52
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.797; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.904; Smooth: 0.907

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (7)

8. Citations (1)

9. Files and Curves (10)