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Crystal structure of octaprenyl pyrophosphate synthase from hyperthermophilic thermotoga maritima

Analyse Crystal structure of octaprenyl pyrophosphate synthase from hyperthermophilic… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1V4E
Type
protein
Length
560 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Octoprenyl-diphosphate synthase
EC
2.5.1.11
UniProt
Q9X1M1
Ligands
SO4
Pockets
10 · best druggability 0.76

Structure

x-ray diffraction · 1 distinct chain · 75% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BOctoprenyl-diphosphate synthase (EC 2.5.1.11)protein28075% helix, 1% strandQ9X1M1

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 7 copies · chains A, B

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

Pockets

10 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15250.760.8360SO4
26310.750.8164SO4
3730.710.9618empty
4570.700.9716empty
52610.580.7722empty

Interfaces

1 interface between chains.

  • A–B · 1746 Ų buried · 14 hydrogen bonds · protein-protein

Compared structures

  • 1V4E · Crystal Structure of Octaprenyl Pyrophosphate Synthase from Hyperthermophilic Thermotoga… · the same entry in another collection · chain A against A, TM-score 1.00

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