Research workbench
Fab fragment of 3D6 in complex with amyloid beta 1-40
Analyse Fab fragment of 3D6 in complex with amyloid beta 1-40 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4ONG
- Type
- protein
- Length
- 429 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 3D6 Fab antibody heavy chain; 3D6 Fab antibody light chain; Amyloid beta A4 protein
- UniProt
- P05067
- Ligands
- ZN, CL
- Pockets
- 2 · best druggability 0.64
Structure
x-ray diffraction · 3 distinct chains · 8% helix, 52% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| H | 3D6 Fab antibody heavy chain | protein | 210 | 9% helix, 53% strand | — |
| L | 3D6 Fab antibody light chain | protein | 214 | 6% helix, 53% strand | — |
| P | Amyloid beta A4 protein | protein | 5 | 60% helix, 0% strand | P05067 |
Ligands and binding sites
- ZN · Zinc ion · metal · 27 copies · chains H, L, P
- CL · Chloride ion · ion · 11 copies · chains H, L
- IMD · Imidazole · additive · 3 copies · chains H, L
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 642 | 0.64 | 0.74 | 64 | ZN, IMD, CL |
| 2 | 141 | 0.43 | 0.76 | 28 | ZN |
Interfaces
3 interfaces between chains.
- H–L · 1779 Ų buried · 17 hydrogen bonds · protein-protein
- H–P · 328 Ų buried · 7 hydrogen bonds · protein-protein
- L–P · 303 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide (disulfide).
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 4ONG · PDBe 4ONG · UniProt P05067
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