MolNFT v1 · #63080 · protein
Crystal structure of anti-human cytomegalovirus antibody 8F9
3EYO · 8F9 Fab: “Crystal structure of anti-human cytomegalovirus antibody 8F9”. X-ray diffraction, 7 pockets (best druggability 0.55). MolNFT v1 #63080 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3EYO
- Type
- protein
- Length
- 857 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 8F9 Fab; Ad-2
- Pockets
- 7 · best druggability 0.55
Structure
x-ray diffraction · 4 distinct chains · 6% helix, 50% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | 8F9 Fab | protein | 213 | 7% helix, 50% strand | — |
| B | Ad-2 | protein | 212 | 4% helix, 51% strand | — |
| C | 8F9 Fab | protein | 214 | 5% helix, 49% strand | — |
| D | Ad-2 | protein | 218 | 7% helix, 50% strand | — |
Pockets
7 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 333 | 0.55 | 0.75 | 38 | empty |
| 2 | 299 | 0.52 | 0.74 | 42 | empty |
| 3 | 85 | 0.34 | 0.74 | 22 | empty |
| 4 | 93 | 0.33 | 0.73 | 20 | empty |
| 5 | 73 | 0.32 | 0.75 | 20 | empty |
Interfaces
3 interfaces between chains.
- C–D · 1712 Ų buried · 12 hydrogen bonds · protein-protein
- A–B · 1623 Ų buried · 8 hydrogen bonds · protein-protein
- B–D · 584 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 9 disulfide (disulfide).
Compared structures
- 3EYO · Crystal structure of anti-human cytomegalovirus antibody 8F9 · the same entry in another collection · chain D against D, 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
- Elsewhere: RCSB PDB 3EYO · PDBe 3EYO
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