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Crystal structure of N-methyl transferase from plasmodium vivax complexed with S-adenosyl methionine and phosphate

Analyse Crystal structure of N-methyl transferase from plasmodium vivax complexed with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4IV0
Type
protein
Length
523 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Phosphoethanolamine N-methyltransferase, putative
EC
2.1.1.103
UniProt
A5K867
Ligands
SAM, PO4
Pockets
6 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 50% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APhosphoethanolamine N-methyltransferase, putative (EC 2.1.1.103)protein26350% helix, 20% strandA5K867
BPhosphoethanolamine N-methyltransferase, putative (EC 2.1.1.103)protein26049% helix, 20% strandA5K867

Ligands and binding sites

  • SAM · S-adenosylmethionine · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · 2 copies · chains A, B
  • BME · Beta-mercaptoethanol · additive · chains B
  • EDO · 1,2-ethanediol · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12250.820.9551PO4, SAM
26880.710.7873SAM
32730.660.8241PO4
41220.510.8123empty
51560.440.7518empty

Interfaces

1 interface between chains.

  • A–B · 197 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (additive adduct).

Compared structures

  • 4IV0 · Crystal structure of N-methyl transferase from Plasmodium vivax complexed with S-adenosyl… · the same entry in another collection · chain A against A, TM-score 1.00

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