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Crystal structure of tryptophan synthase from salmonella typhimurium in complex with N-(4'-trifluoromethoxybenzoyl)-2-amino-1- ethylphosphate (F6F) inhibitor in the alpha-site and beta-site.

Analyse Crystal structure of tryptophan synthase from salmonella typhimurium in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Y6G
Type
protein
Length
653 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tryptophan synthase alpha chain; Tryptophan synthase beta chain
EC
4.2.1.20
UniProt
P00929, P0A2K1
Ligands
F6F, PLP, NA
Pockets
6 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 49% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATryptophan synthase alpha chain (EC 4.2.1.20)protein25751% helix, 14% strandP00929
BTryptophan synthase beta chain (EC 4.2.1.20)protein39647% helix, 20% strandP0A2K1

Ligands and binding sites

  • F6F · 2-{[4-(trifluoromethoxy)benzoyl]amino}ethyl dihydrogen phosphate · ligand · 2 copies · chains A, B
  • PLP · Pyridoxal-5'-phosphate · ligand · chains B
  • NA · Sodium ion · metal · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14590.790.8780PLP, F6F
22740.720.8644F6F
3980.430.7714empty
4680.410.8121empty
5660.360.7814empty

Interfaces

1 interface between chains.

  • A–B · 1401 Ų buried · 26 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 cofactor (pyridoxal phosphate Schiff base).

Compared structures

  • 4Y6G · Crystal structure of Tryptophan Synthase from Salmonella typhimurium in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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