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The structure of plasmodium falciparum spermidine synthase in complex with 5'-methylthioadenosine and N-(3-aminopropyl)-trans-cyclohexane- 1,4-diamine

Analyse The structure of plasmodium falciparum spermidine synthase in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3RIE
Type
protein
Length
841 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Spermidine synthase
EC
2.5.1.16
UniProt
Q8II73
Ligands
MTA, JFQ, 1PG
Pockets
12 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CSpermidine synthase (EC 2.5.1.16)protein28131% helix, 30% strandQ8II73
BSpermidine synthase (EC 2.5.1.16)protein27933% helix, 30% strandQ8II73

Ligands and binding sites

  • MTA · 5'-deoxy-5'-methylthioadenosine · ligand · 3 copies · chains A, B, C
  • JFQ · trans-N-(3-aminopropyl)cyclohexane-1,4-diamine · ligand · 3 copies · chains A, B, C
  • 1PG · 2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol · ligand · chains B, C
  • GOL · Glycerol · additive · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11620.830.9828empty
21380.800.9740MTA, JFQ
31770.790.9444MTA, JFQ
42110.780.9250MTA, JFQ
52850.570.7729empty

Interfaces

2 interfaces between chains.

  • B–C · 1479 Ų buried · 25 hydrogen bonds · protein-protein
  • A–B · 493 Ų buried · 6 hydrogen bonds · protein-protein

Compared structures

  • 3RIE · The structure of Plasmodium falciparum spermidine synthase in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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