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Strictosidine Synthase from Catharanthus roseus in complex with racemic 1-methyl-2,3,4,9-tetrahydro-1H-beta-carboline

Analyse Strictosidine Synthase from Catharanthus roseus in complex with racemic… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6ZEA
Type
protein
Length
308 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.54
Source
Catharanthus roseus
Molecule
Strictosidine synthase
EC
4.3.3.2
UniProt
P18417
Ligands
QGH, QGK
Pockets
2 · best druggability 0.67

Structure

x-ray diffraction · resolution 1.54 · 1 distinct chain · 8% helix, 46% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AStrictosidine synthase (EC 4.3.3.2)protein3088% helix, 46% strandP18417

Ligands and binding sites

  • QGH · (1~{R})-1-methyl-2,3,4,9-tetrahydro-1~{H}-pyrido[3,4-b]indole · ligand · chains A
  • QGK · (1~{S})-1-methyl-2,3,4,9-tetrahydro-1~{H}-pyrido[3,4-b]indole · ligand · chains A
  • EDO · 1,2-ethanediol · additive · 4 copies · 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13240.670.8130QGH, QGK
21650.550.8126EDO

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 6ZEA · Strictosidine synthase from catharanthus roseus in complex with racemic… · the same entry in another collection · chain A against A, TM-score 1.00
  • P18417 · AlphaFold monomer V2.0 prediction for strictosidine synthase (P18417) · a predicted model of the same protein · chain A against A, TM-score 0.98

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