MolNFT v1 · #189007 · protein
Structure of the il-25-il-17RB-il-17RA ternary complex
7UWL · Interleukin-25: “Structure of the il-25-il-17RB-il-17RA ternary complex”. Electron microscopy, 1 ligand (NAG), 20 pockets (best druggability 0.79). MolNFT v1 #189007 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7UWL
- Type
- protein
- Length
- 1,236 residues
- Chains
- 6
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Interleukin-25; Interleukin-17 receptor B; Interleukin-17 receptor a
- UniProt
- Q9H293, Q9NRM6, Q96F46
- Ligands
- NAG
- Pockets
- 20 · best druggability 0.79
Structure
electron microscopy · 4 distinct chains · 5% helix, 39% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Interleukin-25 | protein | 96 | 3% helix, 46% strand | Q9H293 |
| C | Interleukin-17 receptor B | protein | 250 | 5% helix, 41% strand | Q9NRM6 |
| D | Interleukin-17 receptor B | protein | 252 | 5% helix, 39% strand | Q9NRM6 |
| E, F | Interleukin-17 receptor a | protein | 271 | 6% helix, 34% strand | Q96F46 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 22 copies · chains C, D, A, B, E, F
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 887 | 0.79 | 0.81 | 89 | NAG |
| 2 | 194 | 0.76 | 0.91 | 32 | empty |
| 3 | 184 | 0.76 | 0.92 | 31 | empty |
| 4 | 85 | 0.73 | 0.95 | 25 | empty |
| 5 | 52 | 0.69 | 0.96 | 18 | empty |
Interfaces
7 interfaces between chains.
- A–B · 1289 Ų buried · 13 hydrogen bonds · protein-protein
- A–C · 1052 Ų buried · 6 hydrogen bonds · protein-protein
- B–D · 1034 Ų buried · 4 hydrogen bonds · protein-protein
- B–C · 991 Ų buried · 14 hydrogen bonds · protein-protein
- A–D · 986 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 26 disulfide, 18 glycan (disulfide, N-glycosylation).
Compared structures
- 7UWL · Structure of the IL-25-IL-17RB-IL-17RA ternary complex · the same entry in another collection · chain F against F, TM-score 1.00
- Q96F46 · AlphaFold monomer V2.0 prediction for interleukin-17 receptor a (Q96F46) · a predicted model of the same protein · chain F against A, TM-score 0.93
- Q9H293 · AlphaFold monomer V2.0 prediction for interleukin-25 (Q9H293) · a predicted model of the same protein · chain B against A, TM-score 0.88
- Q9NRM6 · AlphaFold monomer V2.0 prediction for interleukin-17 receptor B (Q9NRM6) · a predicted model of the same protein · chain C against A, TM-score 0.79
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 Q9H293
- Every structure of UniProt Q9NRM6
- Every structure of UniProt Q96F46
- Elsewhere: RCSB PDB 7UWL · PDBe 7UWL · UniProt Q9H293 · UniProt Q9NRM6 · UniProt Q96F46
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