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Crystal structure of the heterocyclic toxin methyltransferase from mycobacterium tuberculosis in complex with substrate 1- hydroxyquinolin-4(1H)-one

Analyse Crystal structure of the heterocyclic toxin methyltransferase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7NOY
Type
protein
Length
215 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uncharacterized protein RV0560C
UniProt
P9WKL5
Ligands
SAH, UK5, NA
Pockets
1 · best druggability 0.75

Structure

x-ray diffraction · 1 distinct chain · 30% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUncharacterized protein RV0560Cprotein21530% helix, 29% strandP9WKL5

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains A
  • UK5 · 1-oxidanylquinolin-4-one · ligand · chains A
  • NA · Sodium ion · metal · 3 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
14880.750.8363SAH, UK5, NA

Compared structures

  • 7NOY · Crystal structure of the heterocyclic toxin methyltransferase from Mycobacterium… · the same entry in another collection · chain A against A, TM-score 1.00
  • P9WKL5 · AlphaFold monomer V2.0 prediction for 2-heptyl-1-hydroxyquinolin-4(1H)-one… · a predicted model of the same protein · chain A against A, TM-score 0.97

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