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Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of catechol-O-methyltransferase (comt): structure with CMPD27B

Analyse Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4XUE
Type
protein
Length
429 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Catechol O-methyltransferase
EC
2.1.1.6
UniProt
P21964
Ligands
43J, SAM, MG
Pockets
2 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 48% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BCatechol O-methyltransferase (EC 2.1.1.6)protein21548% helix, 20% strandP21964
ACatechol O-methyltransferase (EC 2.1.1.6)protein21448% helix, 20% strandP21964

Ligands and binding sites

  • 43J · 2-(biphenyl-3-yl)-5-hydroxy-3-methylpyrimidin-4(3H)-one · ligand · 2 copies · chains B, A
  • SAM · S-adenosylmethionine · ligand · 2 copies · chains B, A
  • MG · Magnesium ion · metal · 2 copies · chains B, A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13880.710.825143J, SAM
21470.600.843243J, SAM

Interfaces

1 interface between chains.

  • B–A · 405 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 4XUE · Synthesis and evaluation of heterocyclic catechol mimics as inhibitors of… · the same entry in another collection · chain B against B, TM-score 1.00
  • P21964 · AlphaFold monomer V2.0 prediction for catechol O-methyltransferase (P21964) · a predicted model of the same protein · chain A against A, TM-score 0.99

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