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Co-crystal structure of toxoplasma gondii prolyl tRNA synthetase (tgprs) in complex with hfg and JE6

Analyse Co-crystal structure of toxoplasma gondii prolyl tRNA synthetase (tgprs) in… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7EVU
Type
protein
Length
964 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Prolyl-tRNA synthetase (prors)
UniProt
A0A7J6JUK2
Ligands
HFG, JE6
Pockets
13 · best druggability 0.81

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProlyl-tRNA synthetase (prors)protein48436% helix, 29% strandA0A7J6JUK2
BProlyl-tRNA synthetase (prors)protein48036% helix, 29% strandA0A7J6JUK2

Ligands and binding sites

  • HFG · 7-bromo-6-chloro-3-{3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl}quinazolin-4(3H)-one · ligand · 2 copies · chains A, B
  • JE6 · ~{N}-[4-[(3~{S})-3-cyano-3-cyclopropyl-2-oxidanylidene-pyrrolidin-1-yl]-6-methyl-pyridin-2-yl]-2-phenyl-ethanamide · ligand · 2 copies · chains A, B
  • MES · 2-(N-morpholino)-ethanesulfonic acid · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110170.810.8286MES
2560.730.9917empty
3560.720.9817empty
45830.720.8061HFG, JE6
56040.700.7959HFG, JE6

Interfaces

1 interface between chains.

  • A–B · 2706 Ų buried · 41 hydrogen bonds · protein-protein

Compared structures

  • 7EVU · Co-crystal Structure of Toxoplasma gondii Prolyl tRNA Synthetase (TgPRS) in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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