MolNFT v1 · #102522 · protein
M. tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase W203F mutant bound to fosmidomycin and NADPH
4OOF · 1-deoxy-D-xylulose 5-phosphate reductoisomerase: “M. tuberculosis 1-deoxy-D-xylulose-5-phosphate reductoisomerase W203F mutant bound to fosmidomycin and NADPH”. X-ray diffraction, 3 ligands (NDP, FOM, MN), 6 pockets (best…
- PDB
- 4OOF
- Type
- protein
- Length
- 756 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- 1-deoxy-D-xylulose 5-phosphate reductoisomerase
- EC
- 1.1.1.267
- UniProt
- I6YAH0
- Ligands
- NDP, FOM, MN
- Pockets
- 6 · best druggability 0.74
Structure
x-ray diffraction · 1 distinct chain · 48% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | 1-deoxy-D-xylulose 5-phosphate reductoisomerase (EC 1.1.1.267) | protein | 378 | 48% helix, 16% strand | I6YAH0 |
Ligands and binding sites
- NDP · Nadph dihydro-nicotinamide-adenine-dinucleotide phosphate · ligand · 2 copies · chains A, B
- FOM · 3-[formyl(hydroxy)amino]propylphosphonic acid · ligand · 2 copies · chains A, B
- MN · Manganese (II) ion · metal · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 424 | 0.74 | 0.84 | 74 | NDP, FOM |
| 2 | 400 | 0.73 | 0.84 | 70 | NDP, FOM |
| 3 | 104 | 0.38 | 0.75 | 16 | empty |
| 4 | 82 | 0.36 | 0.75 | 16 | empty |
| 5 | 56 | 0.28 | 0.74 | 14 | empty |
Interfaces
1 interface between chains.
- A–B · 1769 Ų buried · 40 hydrogen bonds · protein-protein
Compared structures
- 4OOF · M. tuberculosis 1-deoxy-d-xylulose-5-phosphate reductoisomerase W203F mutant bound to… · 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 I6YAH0
- Elsewhere: RCSB PDB 4OOF · PDBe 4OOF · UniProt I6YAH0
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