MolNFT v1 · #68439 · protein
Crystal structure of bacillus anthracis dihydrofolate reductase complexed with NADPH and 2,4-diamino-5-(3-(3,4,5-trimethoxyphenyl) prop-1-ynyl)-6-ethylpyrimidine (UCP120A)
3JVX: “Crystal structure of bacillus anthracis dihydrofolate reductase complexed with NADPH and…”. X-ray diffraction, 2 ligands (NDP, EKB), 3 pockets (best druggability 0.71). MolNFT v1 #68439 on GenesisL1: 3D structure, binding sites and…
- PDB
- 3JVX
- Type
- protein
- Length
- 332 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Dihydrofolate reductase
- EC
- 1.5.1.3
- UniProt
- Q81R22
- Ligands
- NDP, EKB
- Pockets
- 3 · best druggability 0.71
Structure
x-ray diffraction · 1 distinct chain · 21% helix, 32% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Dihydrofolate reductase (EC 1.5.1.3) | protein | 166 | 21% helix, 32% strand | Q81R22 |
Ligands and binding sites
- NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
- EKB · 6-ethyl-5-[3-(3,4,5-trimethoxyphenyl)prop-1-yn-1-yl]pyrimidine-2,4-diamine · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 421 | 0.71 | 0.82 | 41 | NDP, EKB |
| 2 | 405 | 0.71 | 0.82 | 42 | NDP, EKB |
| 3 | 574 | 0.71 | 0.79 | 40 | empty |
Interfaces
1 interface between chains.
- A–B · 474 Ų buried · 7 hydrogen bonds · protein-protein
Compared structures
- 3JVX · Crystal structure of Bacillus anthracis dihydrofolate reductase complexed with NADPH and… · the same entry in another collection · 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 Q81R22
- Elsewhere: RCSB PDB 3JVX · PDBe 3JVX · UniProt Q81R22
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