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Wesselsbron virus methyltransferase in complex with adomet and 7MEGPPPG

Analyse Wesselsbron virus methyltransferase in complex with adomet and 7MEGPPPG in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3EMB
Type
protein
Length
260 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Methyltransferase
EC
2.1.1.57
UniProt
C8XPB0
Ligands
SAM, GTG, SO4
Pockets
1 · best druggability 0.66

Structure

x-ray diffraction · 1 distinct chain · 38% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMethyltransferase (EC 2.1.1.57)protein26038% helix, 18% strandC8XPB0

Ligands and binding sites

  • SAM · S-adenosylmethionine · ligand · chains A
  • GTG · 7-methyl-guanosine-5'-triphosphate-5'-guanosine · ligand · chains A
  • SO4 · Sulfate ion · ion · 2 copies · chains A

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15550.660.7756SAM, SO4

Compared structures

  • 3EMB · Wesselsbron virus Methyltransferase in complex with AdoMet and 7MeGpppG · the same entry in another collection · chain A against A, TM-score 1.00

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