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The crystal structure of spermidine synthase from P. falciparum in complex with 5'-methylthioadenosine

Analyse The crystal structure of spermidine synthase from P. falciparum 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
2HTE
Type
protein
Length
823 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, 1PG, UNX, SO4
Pockets
11 · best druggability 0.83

Structure

x-ray diffraction · 3 distinct chains · 32% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASpermidine synthase (EC 2.5.1.16)protein27231% helix, 31% strandQ8II73
BSpermidine synthase (EC 2.5.1.16)protein27031% helix, 32% strandQ8II73
CSpermidine synthase (EC 2.5.1.16)protein28132% helix, 30% strandQ8II73

Ligands and binding sites

  • MTA · 5'-deoxy-5'-methylthioadenosine · ligand · 3 copies · chains A, B, C
  • 1PG · 2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethanol · ligand · 2 copies · chains A, B, C
  • UNX · Unknown atom or ion · ion · 13 copies · chains A, B, C
  • SO4 · Sulfate ion · ion · chains B

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
11680.830.9828empty
21110.770.9638MTA
34060.710.8245MTA
42930.640.8139MTA
54290.620.7744empty

Interfaces

2 interfaces between chains.

  • B–C · 1505 Ų buried · 26 hydrogen bonds · protein-protein
  • A–B · 482 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 2HTE · The crystal structure of spermidine synthase from p. falciparum in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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