MolNFT v1 · #30829 · protein
Mineralocorticoid receptor double mutant with bound cortisone
2AAX: “Mineralocorticoid receptor double mutant with bound cortisone”. X-ray diffraction, 2 ligands (PDN, SO4), 8 pockets (best druggability 0.84). MolNFT v1 #30829 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 2AAX
- Type
- protein
- Length
- 518 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Mineralocorticoid receptor
- UniProt
- P08235
- Ligands
- PDN, SO4
- Pockets
- 8 · best druggability 0.84
Structure
x-ray diffraction · 2 distinct chains · 68% helix, 5% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Mineralocorticoid receptor | protein | 261 | 67% helix, 5% strand | P08235 |
| B | Mineralocorticoid receptor | protein | 257 | 68% helix, 5% strand | P08235 |
Ligands and binding sites
- PDN · 17,21-dihydroxypregna-1,4-diene-3,11,20-trione · ligand · 2 copies · chains A, B
- SO4 · Sulfate ion · ion · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 176 | 0.84 | 0.98 | 23 | PDN |
| 2 | 184 | 0.84 | 0.97 | 24 | PDN |
| 3 | 128 | 0.71 | 0.91 | 20 | empty |
| 4 | 140 | 0.66 | 0.87 | 20 | empty |
| 5 | 189 | 0.50 | 0.76 | 26 | empty |
Interfaces
1 interface between chains.
- A–B · 777 Ų buried · 13 hydrogen bonds · protein-protein
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 P08235
- Elsewhere: RCSB PDB 2AAX · PDBe 2AAX · UniProt P08235
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.