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Dengue 3 NS5 methyltransferase bound to S-adenosyl methionine and molecule BF287

Analyse Dengue 3 NS5 methyltransferase bound to S-adenosyl methionine and molecule BF287 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5EHI
Type
protein
Length
512 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NS5 methyltransferase dengue virus
EC
3.4.21.91, 3.6.1.15, 3.6.4.13, 2.1.1.56, 2.1.1.57, 2.7.7.48
UniProt
P27915
Ligands
SAM, 5O3
Pockets
4 · best druggability 0.67

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CNS5 methyltransferase dengue virus (EC 3.4.21.91, 3.6.1.15, 3.6.4.13, 2.1.1.56, 2.1.1.57, 2.7.7.48)protein25637% helix, 16% strandP27915

Ligands and binding sites

  • SAM · S-adenosylmethionine · ligand · 2 copies · chains A, C
  • 5O3 · 4-[[3-[(2-azanyl-4-chloranyl-phenyl)carbamoylamino]phenyl]sulfonylamino]benzoic acid · ligand · chains A

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15720.670.7756SAM
25570.650.7647SAM
3630.490.8522empty
4920.420.7926empty

Interfaces

1 interface between chains.

  • A–C · 526 Ų buried · 7 hydrogen bonds · protein-protein

Compared structures

  • 5EHI · Dengue 3 NS5 methyltransferase bound to S-adenosyl methionine and molecule BF287 · the same entry in another collection · chain A against A, TM-score 1.00

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