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Crystal structure of an aromatic prenyltransferase FAMD1 from fischerella ambigua utex 1903 in complex with inn

Analyse Crystal structure of an aromatic prenyltransferase FAMD1 from fischerella… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5YNU
Type
protein
Length
607 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aromatic prenyltransferase
UniProt
V5TDY7
Ligands
8XL, POP, DMA
Pockets
6 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAromatic prenyltransferaseprotein29637% helix, 26% strandV5TDY7
BAromatic prenyltransferaseprotein31137% helix, 26% strandV5TDY7

Ligands and binding sites

  • 8XL · 3-[(Z)-2-isocyanoethenyl]-1H-indole · ligand · 2 copies · chains A, B
  • POP · Pyrophosphate 2- · ligand · chains A
  • DMA · Dimethylallyl diphosphate · ligand · chains B
  • IMD · Imidazole · additive · 5 copies · chains A, B
  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13330.810.9156DMA, 8XL
24830.770.85638XL, IMD, POP
34150.680.8048IMD
41980.470.7537IMD
5820.340.7516empty

Interfaces

1 interface between chains.

  • A–B · 470 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 5YNU · Crystal structure of an aromatic prenyltransferase FAMD1 from Fischerella ambigua UTEX… · the same entry in another collection · chain A against A, TM-score 1.00

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