MolNFT v1 · #47983 · protein
Complex of aldose reductase with NADP+ and simaltaneously bound competetive inhibitors fidarestat and IDD594. concentration of fidarestat in soaking solution is equal to concentration of IDD594.
2PF8: “Complex of aldose reductase with NADP+ and simaltaneously bound competetive inhibitors fidarestat and IDD594.…”. X-ray diffraction, 4 ligands (NDP, LDT, FID), 1 pocket (best druggability 0.74). MolNFT v1 #47983 on GenesisL1: 3D…
- PDB
- 2PF8
- Type
- protein
- Length
- 316 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Aldose reductase
- EC
- 1.1.1.21
- UniProt
- P15121
- Ligands
- NDP, LDT, FID, CL
- Pockets
- 1 · best druggability 0.74
Structure
x-ray diffraction · 1 distinct chain · 38% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Aldose reductase (EC 1.1.1.21) | protein | 316 | 38% helix, 15% strand | P15121 |
Ligands and binding sites
- NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · chains A
- LDT · Idd594 · ligand · chains A
- FID · (2S,4S)-2-aminoformyl-6-fluoro-spiro[chroman-4,4'-imidazolidine]-2',5'-dione · ligand · chains A
- CL · Chloride ion · ion · chains A
- CIT · Citric acid · additive · 2 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 319 | 0.74 | 0.85 | 45 | NDP, LDT, FID |
Modifications
Observed in the structure: 2 covalent (additive adduct).
Compared structures
- 2PF8 · Complex of Aldose Reductase with NADP+ and simaltaneously bound competetive inhibitors… · the same entry in another collection · chain A against A, TM-score 1.00
- P15121 · AlphaFold monomer V2.0 prediction for aldo-keto reductase family 1 member B1 (P15121) · a predicted model of the same protein · chain A against A, TM-score 1.00
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 P15121
- Elsewhere: RCSB PDB 2PF8 · PDBe 2PF8 · UniProt P15121
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