9xd0

Structure of a membrane-bound inositol phosphorylceramide synthase and Aureobasidin A complex

Method: ELECTRON MICROSCOPY Dmax: 84.3 Å Quality: GOOD

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

Inositol phosphorylceramide synthase catalytic subunit AUR1

Saccharomyces cerevisiae S288C

UniProt P36107

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: dimeric(2) Count mismatch; review required Chain A; UniProt 1–401 Not recorded Inositol phosphorylceramide synthase regulatory subunit KEI1 × 1 (Q06346) Aureobasidin-A × 1 C14 TETRADECANE × 2 46E (2R)-3-{[(S)-(2-aminoethoxy)(hydroxy)phosphoryl]oxy}-2-(tetradecanoyloxy)propyl tetradecanoate × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.53 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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name AUR1_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–401; UniProt 1–401

Inositol phosphorylceramide synthase regulatory subunit KEI1

Saccharomyces cerevisiae S288C

UniProt Q06346

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: dimeric(2) Count mismatch; review required Chain B; UniProt 1–221 Not recorded Inositol phosphorylceramide synthase catalytic subunit AUR1 × 1 (P36107) Aureobasidin-A × 1 C14 TETRADECANE × 2 46E (2R)-3-{[(S)-(2-aminoethoxy)(hydroxy)phosphoryl]oxy}-2-(tetradecanoyloxy)propyl tetradecanoate × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.53 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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name KEI1_YEAST
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–221; UniProt 1–221

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 9xd0

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9xd0
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9xd0
Deposition date deposition_date2025-10-26
Structure title titleStructure of a membrane-bound inositol phosphorylceramide synthase and Aureobasidin A complex
Keywords keywordsmembrane protein, inositol phosphorylceramide synthase, LIPID BINDING PROTEIN, TRANSFERASE; TRANSFERASE
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier24.28
Radius of gyration Rg (electron density) rg_electron23.48
Forward intensity I(0) i073616400.00
Molecular weight molecular_weight49404.0 kDa
Excluded volume excluded_volume50347 ų
Envelope volume envelope_volume83252 ų
Hydration-shell volume shell_volume29039 ų
Envelope diameter envelope_diameter88.0
Shell Rg shell_rg31.16
Envelope Rg envelope_rg23.83
Shape Rg shape_rg23.50
Total Rg total_rg24.19
Total atoms total_atoms3781
Residues n_residues448
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 dmax84.3
Rg (real space) rg_real24.20
Rg uncertainty (real space) rg_real_error0.57
I(0) (real space) i0_real7.3620e+07
I(0) uncertainty (real space) i0_real_error1.1320e+06
Rg (reciprocal space) rg_reciprocal24.22
I(0) (reciprocal space) i0_reciprocal73620000.0000
Solution quality estimate total_estimate0.8663
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary29.4
Skewness Skewness skewness0.279
Kurtosis Kurtosis kurtosis-0.302
Angular range angular_range— – 0.3250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha17380000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.764; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.973; Smooth: 0.993

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)