MolNFT v1 · #126269 · protein
Coiled-coil protein
5LXN · Transforming acidic coiled-coil-containing protein 3: “Coiled-coil protein”. X-ray diffraction, 1 ligand (SO4), 6 pockets (best druggability 0.67). MolNFT v1 #126269 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 5LXN
- Type
- protein
- Length
- 639 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Transforming acidic coiled-coil-containing protein 3
- UniProt
- Q9Y6A5
- Ligands
- SO4
- Pockets
- 6 · best druggability 0.67
Structure
x-ray diffraction · 4 distinct chains · 95% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C, E | Transforming acidic coiled-coil-containing protein 3 | protein | 81 | 95% helix, 0% strand | Q9Y6A5 |
| B, D, H | Transforming acidic coiled-coil-containing protein 3 | protein | 80 | 95% helix, 0% strand | Q9Y6A5 |
| F | Transforming acidic coiled-coil-containing protein 3 | protein | 76 | 96% helix, 0% strand | Q9Y6A5 |
| G | Transforming acidic coiled-coil-containing protein 3 | protein | 80 | 95% helix, 0% strand | Q9Y6A5 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 2 copies · chains C, D, H
- PGE · Triethylene glycol · additive · 7 copies · chains A, G, H, B, F, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 564 | 0.67 | 0.77 | 49 | PGE |
| 2 | 362 | 0.61 | 0.77 | 49 | PGE |
| 3 | 286 | 0.55 | 0.76 | 37 | PGE |
| 4 | 185 | 0.53 | 0.78 | 23 | empty |
| 5 | 77 | 0.36 | 0.76 | 18 | empty |
Interfaces
18 interfaces between chains.
- C–D · 1873 Ų buried · 11 hydrogen bonds · protein-protein
- A–B · 1837 Ų buried · 6 hydrogen bonds · protein-protein
- E–F · 1829 Ų buried · 4 hydrogen bonds · protein-protein
- G–H · 1702 Ų buried · 5 hydrogen bonds · protein-protein
- B–F · 1081 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 modified, 2 disulfide (engineered, 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 Q9Y6A5
- Elsewhere: RCSB PDB 5LXN · PDBe 5LXN · UniProt Q9Y6A5
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