9ijz

Wild type Homo sapiens Xenotropic and Polytropic Retrovirus Receptor 1 (XPR1)

Method: ELECTRON MICROSCOPY Dmax: 115.7 Å Quality: GOOD

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

Solute carrier family 53 member 1

Homo sapiens

UniProt Q9UBH6

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–696 Chain B; UniProt 1–696 Not recorded PO4 PHOSPHATE ION × 2 6PL (4S,7R)-4-HYDROXY-N,N,N-TRIMETHYL-9-OXO-7-[(PALMITOYLOXY)METHYL]-3,5,8-TRIOXA-4-PHOSPHAHEXACOSAN-1-AMINIUM 4-OXIDE × 2 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.91 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.

50 other PDB entries and 53 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name S53A1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–696; UniProt 1–696 Author chain B; PDBConstruct 1–696; UniProt 1–696

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 9ijz

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9ijz
Deposition date deposition_date2024-06-25
Structure title titleWild type Homo sapiens Xenotropic and Polytropic Retrovirus Receptor 1 (XPR1)
Keywords keywordsPi exporter, a key regulator of cellular Pi homeostasis, PROTEIN TRANSPORT; PROTEIN TRANSPORT
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier35.60
Radius of gyration Rg (electron density) rg_electron34.70
Forward intensity I(0) i0109350000.00
Molecular weight molecular_weight93845.0 kDa
Excluded volume excluded_volume121440 ų
Envelope volume envelope_volume154750 ų
Hydration-shell volume shell_volume37970 ų
Envelope diameter envelope_diameter118.2
Shell Rg shell_rg40.14
Envelope Rg envelope_rg34.31
Shape Rg shape_rg34.69
Total Rg total_rg35.18
Total atoms total_atoms6818
Residues n_residues784
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 dmax115.7
Rg (real space) rg_real35.72
Rg uncertainty (real space) rg_real_error1.20
I(0) (real space) i0_real1.0940e+08
I(0) uncertainty (real space) i0_real_error2.0530e+06
Rg (reciprocal space) rg_reciprocal35.65
I(0) (reciprocal space) i0_reciprocal109300000.0000
Solution quality estimate total_estimate0.8777
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary34.2
Skewness Skewness skewness0.314
Kurtosis Kurtosis kurtosis-0.702
Angular range angular_range— – 0.2200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha10040000.0000
Real-space data points n_real_points45
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.895; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.885; Smooth: 0.837

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)