Research workbench
TCR mimic antibody (Fab fragment) in complex with AFP/HLA-A*02
Analyse TCR mimic antibody (Fab fragment) in complex with AFP/HLA-A*02 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7RE7
- Type
- protein
- Length
- 1,623 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Fab heavy chain; Fab light chain; MHC class I antigen; Beta-2-microglobulin…
- UniProt
- Q861F7, P61769
- Pockets
- 19 · best druggability 0.77
Structure
x-ray diffraction · 7 distinct chains · 14% helix, 46% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| I | Fab heavy chain | protein | 218 | 4% helix, 50% strand | — |
| J, L | Fab light chain | protein | 211 | 6% helix, 51% strand | — |
| H | Fab heavy chain | protein | 212 | 4% helix, 51% strand | — |
| A | MHC class I antigen | protein | 276 | 26% helix, 40% strand | Q861F7 |
| B, E | Beta-2-microglobulin | protein | 100 | 0% helix, 49% strand | P61769 |
| D | MHC class I antigen | protein | 277 | 28% helix, 40% strand | Q861F7 |
| C, F | Phe-met-asn-lys-phe-ile-tyr-glu-ile | protein | 9 | 0% helix, 0% strand | — |
Ligands and binding sites
- GOL · Glycerol · additive · 7 copies · chains I, H, A, D, E
- PG4 · Tetraethylene glycol · additive · 4 copies · chains H, A, B, D, E
- EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · 3 copies · chains I, J, H, L, A, B
- PGE · Triethylene glycol · additive · 2 copies · chains B, D, E
- P6G · Hexaethylene glycol · additive · chains A, B
- 1PE · Pentaethylene glycol · additive · chains D
- FMT · Formic acid · additive · chains D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
19 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1003 | 0.77 | 0.79 | 99 | PG4 |
| 2 | 611 | 0.68 | 0.77 | 60 | P6G |
| 3 | 590 | 0.67 | 0.77 | 59 | FMT, PG4 |
| 4 | 441 | 0.63 | 0.77 | 51 | empty |
| 5 | 516 | 0.61 | 0.74 | 59 | EPE |
Interfaces
17 interfaces between chains.
- H–L · 1641 Ų buried · 15 hydrogen bonds · protein-protein
- I–J · 1631 Ų buried · 15 hydrogen bonds · protein-protein
- D–E · 1439 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 1405 Ų buried · 21 hydrogen bonds · protein-protein
- D–F · 954 Ų buried · 12 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 14 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 Q861F7
- Every structure of UniProt P61769
- Elsewhere: RCSB PDB 7RE7 · PDBe 7RE7 · UniProt Q861F7 · UniProt P61769
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