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MolNFT v1 · #59887 · protein

Functional and structural characterization of a cationdependent O- methyltransferase from the cyanobacterium synechocystis sp. strain pcc 6803

3CBG · O-methyltransferase: “Functional and structural characterization of a cationdependent O- methyltransferase from the cyanobacterium…”. X-ray diffraction, 4 ligands (SAH, FER, 4FE), 1 pocket (best druggability 0.51). MolNFT v1 #59887…

PDB
3CBG
Type
protein
Length
218 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
O-methyltransferase
EC
2.1.1.-
UniProt
Q55813
Ligands
SAH, FER, 4FE, MG
Pockets
1 · best druggability 0.51

Structure

x-ray diffraction · 1 distinct chain · 46% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AO-methyltransferase (EC 2.1.1.-)protein21846% helix, 21% strandQ55813

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains A
  • FER · 3-(4-hydroxy-3-methoxyphenyl)-2-propenoic acid · ligand · chains A
  • 4FE · (2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoic acid · ligand · chains A
  • MG · Magnesium ion · metal · 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
11510.510.7929SAH, FER, 4FE

Compared structures

  • 3CBG · Functional and Structural Characterization of a Cationdependent O-Methyltransferase from… · the same entry in another collection · chain A against A, TM-score 1.00

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