MolNFT v1 · #97835 · protein
Crystal structure of farnesyl synthase mutant (Y204A) complexed with mg, alendronate and isopentenyl pyrophosphate
4KQU · Farnesyl pyrophosphate synthase: “Crystal structure of farnesyl synthase mutant (Y204A) complexed with mg, alendronate and isopentenyl…”. X-ray diffraction, 3 ligands (IPE, AHD, MG), 3 pockets (best druggability 0.82). MolNFT v1…
- PDB
- 4KQU
- Type
- protein
- Length
- 340 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Farnesyl pyrophosphate synthase
- EC
- 2.5.1.10, 2.5.1.1
- UniProt
- P14324
- Ligands
- IPE, AHD, MG
- Pockets
- 3 · best druggability 0.82
Structure
x-ray diffraction · 1 distinct chain · 75% helix, 1% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Farnesyl pyrophosphate synthase (EC 2.5.1.10, 2.5.1.1) | protein | 340 | 75% helix, 1% strand | P14324 |
Ligands and binding sites
- IPE · 3-methylbut-3-enyl trihydrogen diphosphate · ligand · chains A
- AHD · 4-amino-1-hydroxybutane-1,1-diyldiphosphonate · ligand · chains A
- MG · Magnesium ion · metal · 3 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 306 | 0.82 | 0.92 | 48 | MG, IPE, AHD |
| 2 | 159 | 0.54 | 0.80 | 31 | empty |
| 3 | 55 | 0.40 | 0.81 | 23 | empty |
Compared structures
- 4KQU · Crystal Structure of Farnesyl Synthase Mutant (Y204A) Complexed with Mg, Alendronate and… · the same entry in another collection · chain A against A, TM-score 1.00
- P14324 · AlphaFold monomer V2.0 prediction for farnesyl pyrophosphate synthase (P14324) · 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 P14324
- Elsewhere: RCSB PDB 4KQU · PDBe 4KQU · UniProt P14324
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.