MolNFT v1 · #117054 · protein
Beta common receptor in complex with a Fab
5DWU · Cytokine receptor common subunit beta: “Beta common receptor in complex with a Fab”. X-ray diffraction, 1 ligand (NAG), 14 pockets (best druggability 0.73). MolNFT v1 #117054 on GenesisL1: 3D structure, binding sites and pockets in…
- PDB
- 5DWU
- Type
- protein
- Length
- 748 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Cytokine receptor common subunit beta; Fab - heavy chain; Fab - light chain
- UniProt
- P32927
- Ligands
- NAG
- Pockets
- 14 · best druggability 0.73
Structure
x-ray diffraction · 4 distinct chains · 4% helix, 35% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Cytokine receptor common subunit beta | protein | 161 | 9% helix, 19% strand | P32927 |
| B | Cytokine receptor common subunit beta | protein | 181 | 0% helix, 44% strand | P32927 |
| H | Fab - heavy chain | protein | 199 | 3% helix, 36% strand | — |
| L | Fab - light chain | protein | 207 | 5% helix, 38% strand | — |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
14 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 118 | 0.73 | 0.93 | 24 | empty |
| 2 | 87 | 0.71 | 0.94 | 24 | empty |
| 3 | 377 | 0.66 | 0.80 | 35 | empty |
| 4 | 121 | 0.66 | 0.88 | 31 | empty |
| 5 | 227 | 0.57 | 0.79 | 35 | empty |
Interfaces
6 interfaces between chains.
- A–B · 1581 Ų buried · 11 hydrogen bonds · protein-protein
- H–L · 1429 Ų buried · 5 hydrogen bonds · protein-protein
- A–H · 440 Ų buried · 8 hydrogen bonds · protein-protein
- B–H · 280 Ų buried · 6 hydrogen bonds · protein-protein
- B–L · 177 Ų buried · 1 hydrogen bond · protein-protein
Modifications
Observed in the structure: 6 disulfide, 2 glycan (disulfide, N-glycosylation).
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 P32927
- Elsewhere: RCSB PDB 5DWU · PDBe 5DWU · UniProt P32927
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