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MolNFT v1 · #184522 · protein

Human prolyl-tRNA synthetase in complex with L-proline

7OSY · Bifunctional GLUTAMATE/PROLINE--tRNA ligase: “Human prolyl-tRNA synthetase in complex with L-proline”. X-ray diffraction, 3 ligands (PRO, SR, ZN), 10 pockets (best druggability 0.74). MolNFT v1 #184522 on GenesisL1: 3D structure…

PDB
7OSY
Type
protein
Length
967 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional GLUTAMATE/PROLINE--tRNA ligase
EC
6.1.1.17, 6.1.1.15
UniProt
P07814
Ligands
PRO, SR, ZN
Pockets
10 · best druggability 0.74

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
ABifunctional GLUTAMATE/PROLINE--tRNA ligase (EC 6.1.1.17, 6.1.1.15)protein48336% helix, 29% strandP07814
BBifunctional GLUTAMATE/PROLINE--tRNA ligase (EC 6.1.1.17, 6.1.1.15)protein48436% helix, 29% strandP07814

Ligands and binding sites

  • PRO · Proline · ligand · 2 copies · chains A, B
  • SR · Strontium ion · metal · 6 copies · chains A, B
  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

10 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15500.740.8246PRO
25070.740.8250PRO
32330.670.8440empty
44050.640.7836SR
52940.590.7826SR

Interfaces

1 interface between chains.

  • A–B · 2269 Ų buried · 30 hydrogen bonds · protein-protein

Compared structures

  • 7OSY · Human Prolyl-tRNA Synthetase in Complex with L-proline · the same entry in another collection · chain A against A, TM-score 1.00
  • P07814 · AlphaFold monomer V2.0 prediction for bifunctional GLUTAMATE/PROLINE --tRNA ligase… · a predicted model of the same protein · chain A against A, TM-score 0.98

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