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Structure of the complex of trypanosoma cruzi farnesyl disphosphate synthase with alendronate, isopentenyl diphosphate and MG+2

Analyse Structure of the complex of trypanosoma cruzi farnesyl disphosphate synthase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YHM
Type
protein
Length
1,086 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Farnesyl pyrophosphate synthase
EC
2.5.1.10
UniProt
Q8WS26
Ligands
AHD, IPE, MG, SO4
Pockets
11 · best druggability 0.81

Structure

x-ray diffraction · 1 distinct chain · 74% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CFarnesyl pyrophosphate synthase (EC 2.5.1.10)protein36274% helix, 1% strandQ8WS26

Ligands and binding sites

  • AHD · 4-amino-1-hydroxybutane-1,1-diyldiphosphonate · ligand · 3 copies · chains A, B, C
  • IPE · 3-methylbut-3-enyl trihydrogen diphosphate · ligand · 3 copies · chains A, B, C
  • MG · Magnesium ion · metal · 9 copies · chains A, B, C
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

11 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12830.810.9347MG, AHD, IPE
22680.810.9346MG, AHD, IPE
32920.810.9246MG, AHD, IPE
4900.780.9921empty
52210.510.7627empty

Interfaces

2 interfaces between chains.

  • A–B · 3167 Ų buried · 44 hydrogen bonds · protein-protein
  • A–C · 346 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 45 modified (engineered).

Compared structures

  • 1YHM · Structure of the complex of Trypanosoma cruzi farnesyl disphosphate synthase with… · the same entry in another collection · chain A against A, TM-score 1.00

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