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Crystal structure of a methyltransferase involved in the biosynthesis of gentamicin in complex with the kanamycin B

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

PDB
5U1E
Type
protein
Length
321 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.213
Source
Micromonospora echinospora
Molecule
Putative gentamicin methyltransferase
UniProt
Q2MG72
Ligands
9CS, SAH
Pockets
2 · best druggability 0.71

Structure

x-ray diffraction · resolution 2.213 · 1 distinct chain · 35% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative gentamicin methyltransferaseprotein32135% helix, 28% strandQ2MG72

Ligands and binding sites

  • 9CS · (1R,2S,3S,4R,6S)-4,6-diamino-3-[(3-amino-3-deoxy-alpha-D-glucopyranosyl)oxy]-2-hydroxycyclohexyl 2,6-diamino-2,6-dideoxy-alpha-D-glucopyranoside · ligand · chains A
  • SAH · S-adenosyl-L-homocysteine · ligand · chains 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12680.710.85449CS, SAH
2530.410.8215empty

Compared structures

  • 5U1E · Crystal structure of a methyltransferase involved in the biosynthesis of gentamicin in… · the same entry in another collection · chain A against A, TM-score 1.00

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