MolNFT v1 · #109287 · protein
Crystal structure of recombinant 4E10 expressed in escherichia COLI with epitope bound
4WY7 · Fab 4E10 heavy chain: “Crystal structure of recombinant 4E10 expressed in escherichia COLI with epitope bound”. X-ray diffraction, 3 pockets (best druggability 0.59). MolNFT v1 #109287 on GenesisL1: 3D structure, binding sites and…
- PDB
- 4WY7
- Type
- protein
- Length
- 447 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Fab 4E10 heavy chain; Fab 4E10LIGHT chain; Envelope glycoprotein GP160
- UniProt
- P05880
- Pockets
- 3 · best druggability 0.59
Structure
x-ray diffraction · 3 distinct chains · 10% helix, 50% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| H | Fab 4E10 heavy chain | protein | 220 | 7% helix, 55% strand | — |
| L | Fab 4E10LIGHT chain | protein | 212 | 7% helix, 49% strand | — |
| P | Envelope glycoprotein GP160 | protein | 15 | 87% helix, 0% strand | P05880 |
Ligands and binding sites
- GOL · Glycerol · additive · 2 copies · chains L, H
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 502 | 0.59 | 0.74 | 61 | empty |
| 2 | 117 | 0.43 | 0.77 | 21 | empty |
| 3 | 74 | 0.32 | 0.74 | 17 | empty |
Interfaces
3 interfaces between chains.
- H–L · 1600 Ų buried · 10 hydrogen bonds · protein-protein
- H–P · 578 Ų buried · 4 hydrogen bonds · protein-protein
- L–P · 213 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide (disulfide).
Compared structures
- 4WY7 · Crystal structure of recombinant 4E10 expressed in Escherichia coli with epitope bound · the same entry in another collection · chain H against H, 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 P05880
- Elsewhere: RCSB PDB 4WY7 · PDBe 4WY7 · UniProt P05880
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