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Apra methyltransferase 1 - gnat in complex with MN2+ , SAM, and di- methyl-malonate

Analyse Apra methyltransferase 1 - gnat in complex with MN2+ , SAM, and di… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7UCH
Type
protein
Length
636 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Apra methyltransferase 1
UniProt
A0A1U7N2Z8
Ligands
MU6, SAH, MN
Pockets
8 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 50% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AApra methyltransferase 1protein63650% helix, 15% strandA0A1U7N2Z8

Ligands and binding sites

  • MU6 · dimethylpropanedioic acid · ligand · chains A
  • SAH · S-adenosyl-L-homocysteine · ligand · chains A
  • MN · Manganese (II) ion · metal · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110090.790.8083MN, GOL, MU6, SAH
22620.610.8030empty
32500.570.7828empty
41730.480.7623empty
51410.440.7619empty

Compared structures

  • 7UCH · AprA Methyltransferase 1 - GNAT in complex with Mn2+ , SAM, and Di-methyl-malonate · the same entry in another collection · chain A against A, TM-score 1.00

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