Research workbench
Crystal structure of the complex between il-13 and M1295 Fab
Analyse Crystal structure of the complex between il-13 and M1295 Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4PS4
- Type
- protein
- Length
- 513 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- M1295 light chain; M1295 heavy chain; Interleukin-13
- UniProt
- P35225
- Pockets
- 5 · best druggability 0.61
Structure
x-ray diffraction · 3 distinct chains · 13% helix, 43% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| L | M1295 light chain | protein | 213 | 6% helix, 51% strand | — |
| H | M1295 heavy chain | protein | 224 | 5% helix, 50% strand | — |
| A | Interleukin-13 | protein | 76 | 59% helix, 0% strand | P35225 |
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 524 | 0.61 | 0.75 | 60 | empty |
| 2 | 54 | 0.53 | 0.89 | 22 | empty |
| 3 | 218 | 0.50 | 0.75 | 38 | empty |
| 4 | 93 | 0.40 | 0.77 | 23 | empty |
| 5 | 86 | 0.32 | 0.74 | 18 | empty |
Interfaces
3 interfaces between chains.
- L–H · 1850 Ų buried · 13 hydrogen bonds · protein-protein
- H–A · 478 Ų buried · 9 hydrogen bonds · protein-protein
- L–A · 206 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide, 1 modified (disulfide, cyclization).
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 P35225
- Elsewhere: RCSB PDB 4PS4 · PDBe 4PS4 · UniProt P35225
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