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The structure of PKMT2 from rickettsia typhi in complex with adohcy

Analyse The structure of PKMT2 from rickettsia typhi in complex with adohcy in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5DPL
Type
protein
Length
1,032 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein lysine methyltransferase 2
UniProt
Q68XQ5
Ligands
SAH
Pockets
15 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein lysine methyltransferase 2protein52043% helix, 12% strandQ68XQ5
BProtein lysine methyltransferase 2protein51241% helix, 14% strandQ68XQ5

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 2 copies · chains A, B

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

Pockets

15 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17020.730.7967SAH
27470.720.7868SAH
3510.680.9713empty
43180.620.7941empty
51750.620.8328empty

Interfaces

1 interface between chains.

  • A–B · 1635 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 5DPL · The structure of PKMT2 from Rickettsia typhi in complex with AdoHcy · the same entry in another collection · chain A against A, TM-score 1.00

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