9d45

Cryo-EM structure of yeast Exportin Msn5 bound to cargo Pho4 and RanGTP

Method: ELECTRON MICROSCOPY Dmax: 117.8 Å Quality: EXCELLENT

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

Protein MSN5

Saccharomyces cerevisiae

UniProt P52918

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 1–1224 Not recorded GTP-binding nuclear protein GSP1/CNR1 × 1 (P32835) Phosphate system positive regulatory protein PHO4 × 1 (P07270) GTP GUANOSINE-5'-TRIPHOSPHATE × 1 MG MAGNESIUM ION × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.10 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.

3 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MSN5_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–1224; UniProt 1–1224

GTP-binding nuclear protein GSP1/CNR1

Saccharomyces cerevisiae

UniProt P32835

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 B; UniProt 2–179 Mutation:Q71L Protein MSN5 × 1 (P52918) Phosphate system positive regulatory protein PHO4 × 1 (P07270) GTP GUANOSINE-5'-TRIPHOSPHATE × 1 MG MAGNESIUM ION × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.10 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.

11 other PDB entries and 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name GSP1_YEAST
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 3–180; UniProt 2–179

Phosphate system positive regulatory protein PHO4

Saccharomyces cerevisiae

UniProt P07270

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 1–200 Non-standard monomer:Yes (specific site not provided by mmCIF) Protein MSN5 × 1 (P52918) GTP-binding nuclear protein GSP1/CNR1 × 1 (P32835) GTP GUANOSINE-5'-TRIPHOSPHATE × 1 MG MAGNESIUM ION × 1 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.4 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 3.10 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 PHO4_YEAST
Isoform
PDB entities 3
Chains and sequence ranges Author chain C; PDBConstruct 3–202; UniProt 1–200

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 9d45

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9d45
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9d45
Deposition date deposition_date2024-08-12
Structure title titleCryo-EM structure of yeast Exportin Msn5 bound to cargo Pho4 and RanGTP
Keywords keywordsKaryopherin, Exportin, Nuclear Export, TRANSPORT PROTEIN; TRANSPORT PROTEIN
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier37.97
Radius of gyration Rg (electron density) rg_electron37.21
Forward intensity I(0) i0348390000.00
Molecular weight molecular_weight157700.0 kDa
Excluded volume excluded_volume199880 ų
Envelope volume envelope_volume267960 ų
Hydration-shell volume shell_volume58758 ų
Envelope diameter envelope_diameter115.9
Shell Rg shell_rg44.92
Envelope Rg envelope_rg35.97
Shape Rg shape_rg37.23
Total Rg total_rg37.64
Total atoms total_atoms11101
Residues n_residues1352
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 dmax117.8
Rg (real space) rg_real37.75
Rg uncertainty (real space) rg_real_error0.87
I(0) (real space) i0_real3.4840e+08
I(0) uncertainty (real space) i0_real_error6.0450e+06
Rg (reciprocal space) rg_reciprocal37.89
I(0) (reciprocal space) i0_reciprocal348400000.0000
Solution quality estimate total_estimate0.9058
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary50.5
Skewness Skewness skewness0.100
Kurtosis Kurtosis kurtosis-0.582
Angular range angular_range— – 0.2100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha73960000.0000
Real-space data points n_real_points43
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.945; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.989; Smooth: 0.946

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)