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R304K trichodiene synthase: complex with mg, pyrophosphate, and (4S)- 7-azabisabolene

Analyse R304K trichodiene synthase: complex with mg, pyrophosphate, and (4S)… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2AET
Type
protein
Length
705 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Trichodiene synthase
EC
4.2.3.6
UniProt
P13513
Ligands
POP, MG
Pockets
11 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 70% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATrichodiene synthase (EC 4.2.3.6)protein35270% helix, 0% strandP13513
BTrichodiene synthase (EC 4.2.3.6)protein35369% helix, 0% strandP13513

Ligands and binding sites

  • POP · Pyrophosphate 2- · ligand · chains B
  • MG · Magnesium ion · metal · 3 copies · chains B
  • EDO · 1,2-ethanediol · additive · 2 copies · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15840.790.8565MG, POP
25990.770.8351empty
3830.750.9818empty
4650.730.9720EDO
53120.620.7938empty

Interfaces

1 interface between chains.

  • A–B · 2778 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 2AET · R304K trichodiene synthase: Complex with Mg, pyrophosphate, and (4S)-7-azabisabolene · the same entry in another collection · chain A against A, TM-score 1.00
  • P13513 · AlphaFold monomer V2.0 prediction for trichodiene synthase (P13513) · a predicted model of the same protein · chain A against A, TM-score 1.00

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