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Structure and activity of a flavonoid 3-O glucosyltransferase reveals the basis for plant natural product modification

Analyse Structure and activity of a flavonoid 3-O glucosyltransferase reveals the basis… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2C1X
Type
protein
Length
434 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Udp-glucose flavonoid 3-O glycosyltransferase
EC
2.4.1.91
UniProt
O22304
Ligands
UDP
Pockets
3 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 49% helix, 14% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUdp-glucose flavonoid 3-O glycosyltransferase (EC 2.4.1.91)protein43449% helix, 14% strandO22304

Ligands and binding sites

  • UDP · Uridine-5'-diphosphate · ligand · chains A
  • B3P · 2-[3-(2-hydroxy-1,1-dihydroxymethyl-ethylamino)-propylamino]-2-hydroxymethyl-propane-1,3-diol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16920.770.8281UDP, B3P
2690.560.8715empty
3910.390.7715empty

Compared structures

  • 2C1X · Structure and activity of a flavonoid 3-O glucosyltransferase reveals the basis for plant… · the same entry in another collection · chain A against A, TM-score 1.00

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