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Crystal structure of leshmaniasis major farnesyl diphosphate synthase in complex with 1-(2-hydroxy-2,2-diphosphonoethyl)-3- phenylpyridinium, ipp and CA2+

Analyse Crystal structure of leshmaniasis major farnesyl diphosphate synthase in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JZB
Type
protein
Length
724 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Farnesyl pyrophosphate synthase
EC
2.5.1.1, 2.5.1.10
UniProt
Q4QBL1
Ligands
IPE, P2H, CA, NA
Pockets
8 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 73% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BFarnesyl pyrophosphate synthase (EC 2.5.1.1, 2.5.1.10)protein36273% helix, 1% strandQ4QBL1

Ligands and binding sites

  • IPE · 3-methylbut-3-enyl trihydrogen diphosphate · ligand · 2 copies · chains A, B
  • P2H · 1-(2-hydroxy-2,2-diphosphonoethyl)-3-phenylpyridinium · ligand · 2 copies · chains A, B
  • CA · Calcium ion · metal · 6 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B

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

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13850.830.9258CA, IPE, P2H
23780.830.9259IPE, P2H, CA
31870.530.7926empty
41410.530.8126empty
51960.500.7624empty

Interfaces

1 interface between chains.

  • A–B · 2955 Ų buried · 42 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (formylation).

Compared structures

  • 4JZB · Crystal Structure of Leshmaniasis major Farnesyl diphosphate synthase in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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