MolNFT v1 · #164281 · protein
Cryo-EM structure of alpha-synuclein fibril polymorph 2A
6SSX: “Cryo-EM structure of alpha-synuclein fibril polymorph 2A”. Electron microscopy, 6 pockets (best druggability 0.39). MolNFT v1 #164281 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 6SSX
- Type
- protein
- Length
- 730 residues
- Chains
- 10
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Alpha-synuclein
- UniProt
- P37840
- Pockets
- 6 · best druggability 0.39
Structure
electron microscopy · 1 distinct chain · 0% helix, 71% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F, G, H, I, J | Alpha-synuclein | protein | 73 | 0% helix, 71% strand | P37840 |
Pockets
6 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 94 | 0.39 | 0.77 | 25 | empty |
| 2 | 91 | 0.37 | 0.76 | 21 | empty |
| 3 | 93 | 0.32 | 0.73 | 19 | empty |
| 4 | 64 | 0.29 | 0.74 | 17 | empty |
| 5 | 63 | 0.29 | 0.74 | 14 | empty |
Interfaces
21 interfaces between chains.
- A–B · 2756 Ų buried · 103 hydrogen bonds · protein-protein
- F–G · 2750 Ų buried · 103 hydrogen bonds · protein-protein
- I–J · 2735 Ų buried · 101 hydrogen bonds · protein-protein
- D–E · 2734 Ų buried · 99 hydrogen bonds · protein-protein
- B–C · 2731 Ų buried · 99 hydrogen bonds · protein-protein
Compared structures
- 6SSX · cryo-em structure of alpha-synuclein fibril polymorph 2A · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P37840
- Elsewhere: RCSB PDB 6SSX · PDBe 6SSX · UniProt P37840
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