8zmy

F0502B-bound WT polymorph 5a alpha-synuclein fibril

Method: ELECTRON MICROSCOPY Dmax: 125.6 Å Quality: GOOD

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

Alpha-synuclein

Homo sapiens

UniProt P37840

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 × 12 PDB declaration: 12-meric(12) Consistent with protein copy count Chain A; UniProt 1–98 Chain B; UniProt 1–98 Chain C; UniProt 1–98 Chain D; UniProt 1–98 Chain E; UniProt 1–98 Chain F; UniProt 1–98 Chain G; UniProt 1–98 Chain H; UniProt 1–98 Chain I; UniProt 1–98 Chain J; UniProt 1–98 Chain K; UniProt 1–98 Chain L; UniProt 1–98 Non-standard monomer:Yes (specific site not provided by mmCIF) 1KI 2-bromanyl-4-[(~{E})-2-[6-[2-(2-fluoranylethoxy)ethyl-methyl-amino]-5-methyl-1,3-benzothiazol-2-yl]ethenyl]phenol × 15 ELECTRON MICROSCOPY cryo-EM buffer:pH 7.5 cryo-EM vitrification conditions:Cryogen ETHANE Resolution 2.90 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.

226 other PDB entries and 234 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SYUA_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–99; UniProt 1–98 Author chain B; PDBConstruct 2–99; UniProt 1–98 Author chain C; PDBConstruct 2–99; UniProt 1–98 Author chain D; PDBConstruct 2–99; UniProt 1–98 Author chain E; PDBConstruct 2–99; UniProt 1–98 Author chain F; PDBConstruct 2–99; UniProt 1–98 Author chain G; PDBConstruct 2–99; UniProt 1–98 Author chain H; PDBConstruct 2–99; UniProt 1–98 Author chain I; PDBConstruct 2–99; UniProt 1–98 Author chain J; PDBConstruct 2–99; UniProt 1–98 Author chain K; PDBConstruct 2–99; UniProt 1–98 Author chain L; PDBConstruct 2–99; UniProt 1–98

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 8zmy

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8zmy
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8zmy
Deposition date deposition_date2024-05-24
Structure title titleF0502B-bound WT polymorph 5a alpha-synuclein fibril
Keywords keywordsamyloid fibril, complex, PROTEIN FIBRIL; PROTEIN FIBRIL
Experimental Method methodELECTRON MICROSCOPY

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

Radius of gyration Rg (Guinier) rg_guinier37.49
Radius of gyration Rg (electron density) rg_electron37.34
Forward intensity I(0) i0228720000.00
Molecular weight molecular_weight124500.0 kDa
Excluded volume excluded_volume156760 ų
Envelope volume envelope_volume192600 ų
Hydration-shell volume shell_volume44572 ų
Envelope diameter envelope_diameter134.9
Shell Rg shell_rg41.61
Envelope Rg envelope_rg37.67
Shape Rg shape_rg37.39
Total Rg total_rg37.41
Total atoms total_atoms8652
Residues n_residues1176
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 dmax125.6
Rg (real space) rg_real37.65
Rg uncertainty (real space) rg_real_error1.01
I(0) (real space) i0_real2.2870e+08
I(0) uncertainty (real space) i0_real_error4.0360e+06
Rg (reciprocal space) rg_reciprocal37.56
I(0) (reciprocal space) i0_reciprocal228700000.0000
Solution quality estimate total_estimate0.8922
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary38.9
Skewness Skewness skewness0.389
Kurtosis Kurtosis kurtosis-0.422
Angular range angular_range— – 0.2100 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha26080000.0000
Real-space data points n_real_points43
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.889; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.948; Smooth: 0.981

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (1)

9. Files and Curves (10)