MolNFT v1 · #16315 · protein
Fructose-1,6-bisphosphatase complex with magnesium, fructose-6- phosphate, phosphate, edta and thallium (20 mm)
1NV6: “Fructose-1,6-bisphosphatase complex with magnesium, fructose-6- phosphate, phosphate, edta and thallium (20…”. X-ray diffraction, 5 ligands (F6P, TL, MG), 2 pockets (best druggability 0.53). MolNFT v1 #16315 on GenesisL1: 3D…
- PDB
- 1NV6
- Type
- protein
- Length
- 329 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Fructose-1,6-bisphosphatase
- EC
- 3.1.3.11
- UniProt
- P00636
- Ligands
- F6P, TL, MG, PO4, PI
- Pockets
- 2 · best druggability 0.53
Structure
x-ray diffraction · 1 distinct chain · 34% helix, 26% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Fructose-1,6-bisphosphatase (EC 3.1.3.11) | protein | 329 | 34% helix, 26% strand | P00636 |
Ligands and binding sites
- F6P · 6-O-phosphono-beta-D-fructofuranose · ligand · chains A
- TL · Thallium (I) ion · metal · 5 copies · chains A
- MG · Magnesium ion · metal · 2 copies · chains A
- PO4 · Phosphate ion · ion · chains A
- PI · Hydrogenphosphate ion · ion · 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 | 120 | 0.53 | 0.82 | 24 | F6P, PI, TL |
| 2 | 123 | 0.42 | 0.76 | 21 | PO4 |
Compared structures
- 1NV6 · Fructose-1,6-Bisphosphatase Complex With Magnesium, Fructose-6-Phosphate, Phosphate, EDTA… · the same entry in another collection · chain A against A, TM-score 1.00
- P00636 · AlphaFold monomer V2.0 prediction for fructose-1,6-bisphosphatase 1 (P00636) · 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 P00636
- Elsewhere: RCSB PDB 1NV6 · PDBe 1NV6 · UniProt P00636
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