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Crystal structure of a M1A58 tRNA methyltransferase

Analyse Crystal structure of a M1A58 tRNA methyltransferase in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2PWY
Type
protein
Length
501 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
TRNA (adenine-N(1)-)-methyltransferase
EC
2.1.1.36
UniProt
Q8GBB2
Ligands
SAH, SO4
Pockets
7 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 30% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATRNA (adenine-N(1)-)-methyltransferase (EC 2.1.1.36)protein25129% helix, 33% strandQ8GBB2
BTRNA (adenine-N(1)-)-methyltransferase (EC 2.1.1.36)protein25030% helix, 34% strandQ8GBB2

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11260.800.9824empty
26410.690.7781empty
31690.490.7735SAH
41600.470.7733SAH
5570.400.8122empty

Interfaces

1 interface between chains.

  • A–B · 2224 Ų buried · 53 hydrogen bonds · protein-protein

Compared structures

  • 2PWY · Crystal Structure of a m1A58 tRNA methyltransferase · the same entry in another collection · chain A against A, TM-score 1.00
  • Q8GBB2 · AlphaFold monomer V2.0 prediction for tRNA (ADENINE(58)-N(1))-methyltransferase trmi… · a predicted model of the same protein · chain A against A, TM-score 0.99

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