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Crystal structure of human fpps in complex with alendronate

Analyse Crystal structure of human fpps in complex with alendronate in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2F92
Type
protein
Length
343 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Farnesyl diphosphate synthase
EC
2.5.1.1, 2.5.1.10
UniProt
P14324
Ligands
AHD, ZN, PO4
Pockets
2 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 76% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
FFarnesyl diphosphate synthase (EC 2.5.1.1, 2.5.1.10)protein34376% helix, 1% strandP14324

Ligands and binding sites

  • AHD · 4-amino-1-hydroxybutane-1,1-diyldiphosphonate · ligand · chains F
  • ZN · Zinc ion · metal · 3 copies · chains F
  • PO4 · Phosphate ion · ion · chains F

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.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14200.780.8758ZN, PO4, AHD
2530.280.7416empty

Compared structures

  • 2F92 · Crystal structure of human FPPS in complex with alendronate · the same entry in another collection · chain F against F, TM-score 1.00
  • P14324 · AlphaFold monomer V2.0 prediction for farnesyl pyrophosphate synthase (P14324) · a predicted model of the same protein · chain F against A, TM-score 1.00

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