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Structure of strictosidine synthase in complex with inhibitor

Analyse Structure of strictosidine synthase in complex with inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2VAQ
Type
protein
Length
610 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Strictosidine synthase
EC
4.3.3.2
UniProt
P68175
Ligands
VAW
Pockets
7 · best druggability 0.72

Structure

x-ray diffraction · 1 distinct chain · 7% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BStrictosidine synthase (EC 4.3.3.2)protein3057% helix, 48% strandP68175

Ligands and binding sites

  • VAW · (2S,3R,4S)-methyl 4-(2-(2-(1H-indol-3-yl)ethylamino)ethyl)-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylate · ligand · 2 copies · chains A, B

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

Pockets

7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13040.720.8533VAW
22480.690.8528VAW
31820.580.8225empty
41930.570.8025empty
51580.470.7622empty

Interfaces

1 interface between chains.

  • A–B · 794 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 2VAQ · Structure of strictosidine synthase in complex with inhibitor · the same entry in another collection · chain A against A, TM-score 1.00
  • P68175 · AlphaFold monomer V2.0 prediction for strictosidine synthase (P68175) · a predicted model of the same protein · chain A against A, TM-score 1.00

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