MolNFT v2 · #146552 · protein
Alpha Synuclein fibril formed by full length protein - Rod Polymorph
6CU7 · Alpha-synuclein: “Alpha Synuclein fibril formed by full length protein - Rod Polymorph”. Electron microscopy at 3.5, 6 pockets (best druggability 0.75). MolNFT v2 #146552 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 6CU7
- Type
- protein
- Length
- 600 residues
- Chains
- 10
- Method
- electron microscopy
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 3.5
- Source
- Homo sapiens
- Molecule
- Alpha-synuclein
- UniProt
- P37840
- Pockets
- 6 · best druggability 0.75
Structure
electron microscopy · resolution 3.5 · 1 distinct chain · 0% helix, 55% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| E, A, B, C, D, F, G, H, I, J | Alpha-synuclein | protein | 60 | 0% helix, 55% strand | P37840 |
Pockets
6 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 632 | 0.75 | 0.82 | 48 | empty |
| 2 | 602 | 0.73 | 0.81 | 47 | empty |
| 3 | 320 | 0.59 | 0.77 | 28 | empty |
| 4 | 301 | 0.55 | 0.76 | 27 | empty |
| 5 | 63 | 0.29 | 0.74 | 17 | empty |
Interfaces
25 interfaces between chains.
- G–I · 2446 Ų buried · 77 hydrogen bonds · protein-protein
- E–C · 2431 Ų buried · 72 hydrogen bonds · protein-protein
- F–H · 2427 Ų buried · 74 hydrogen bonds · protein-protein
- D–F · 2425 Ų buried · 70 hydrogen bonds · protein-protein
- H–J · 2415 Ų buried · 68 hydrogen bonds · protein-protein
Compared structures
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 6CU7 · PDBe 6CU7 · UniProt P37840
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