MolNFT v1 · #8936 · protein
Comparison of ternary crystal complexes of human dihydrofolate reductase with NADPH and a classical antitumor furopyrimdine
1HFR: “Comparison of ternary crystal complexes of human dihydrofolate reductase with NADPH and a classical antitumor…”. X-ray diffraction, 2 ligands (NDP, MOT), 2 pockets (best druggability 0.74). MolNFT v1 #8936 on GenesisL1: 3D…
- PDB
- 1HFR
- Type
- protein
- Length
- 186 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Dihydrofolate reductase
- EC
- 1.5.1.3
- UniProt
- P00374
- Ligands
- NDP, MOT
- Pockets
- 2 · best druggability 0.74
Structure
x-ray diffraction · 1 distinct chain · 23% helix, 34% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Dihydrofolate reductase (EC 1.5.1.3) | protein | 186 | 23% helix, 34% strand | P00374 |
Ligands and binding sites
- NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · chains A
- MOT · N-[4-[(2,4-diaminofuro[2,3d]pyrimidin-5-yl)methyl]methylamino]-benzoyl]-L-glutamate · ligand · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 340 | 0.74 | 0.86 | 38 | NDP, MOT |
| 2 | 52 | 0.25 | 0.73 | 17 | NDP |
Compared structures
- 1HFR · Comparison of ternary crystal complexes of human dihydrofolate reductase with NADPH and a… · the same entry in another collection · chain A against A, TM-score 1.00
- P00374 · AlphaFold monomer V2.0 prediction for dihydrofolate reductase (P00374) · a predicted model of the same protein · chain A against A, TM-score 0.99
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 P00374
- Elsewhere: RCSB PDB 1HFR · PDBe 1HFR · UniProt P00374
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.