MolNFT v1 · #185634 · protein
Type II beta-amyloid 42 filaments from human brain
7Q4M · Amyloid-beta precursor protein: “Type II beta-amyloid 42 filaments from human brain”. Electron microscopy, 1 ligand (UNX), 2 pockets (best druggability 0.28). MolNFT v1 #185634 on GenesisL1: 3D structure, binding sites and pockets…
- PDB
- 7Q4M
- Type
- protein
- Length
- 310 residues
- Chains
- 10
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Amyloid-beta precursor protein
- UniProt
- P05067
- Ligands
- UNX
- Pockets
- 2 · best druggability 0.28
Structure
electron microscopy · 1 distinct chain · 0% helix, 61% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D, E, F, G, H, I, J | Amyloid-beta precursor protein | protein | 31 | 0% helix, 61% strand | P05067 |
Ligands and binding sites
- UNX · Unknown atom or ion · ion · 10 copies · chains A, C, B, D, E, F, G, H, I, J
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 78 | 0.28 | 0.73 | 20 | empty |
| 2 | 70 | 0.26 | 0.72 | 20 | empty |
Interfaces
21 interfaces between chains.
- B–D · 1234 Ų buried · 36 hydrogen bonds · protein-protein
- B–H · 1223 Ų buried · 32 hydrogen bonds · protein-protein
- D–F · 1220 Ų buried · 34 hydrogen bonds · protein-protein
- A–C · 1219 Ų buried · 33 hydrogen bonds · protein-protein
- G–I · 1216 Ų buried · 32 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 P05067
- Elsewhere: RCSB PDB 7Q4M · PDBe 7Q4M · UniProt P05067
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