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Editing domain of threonyl-tRNA synthetase from Methanococcus jannaschii with L-Thr3AA

Analyse Editing domain of threonyl-tRNA synthetase from Methanococcus jannaschii with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RRG
Type
protein
Length
551 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.93
Source
Methanocaldococcus jannaschii
Molecule
Threonine--tRNA ligase
EC
6.1.1.3
UniProt
Q58597
Ligands
A3T
Pockets
7 · best druggability 0.77

Structure

x-ray diffraction · resolution 1.93 · 2 distinct chains · 32% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, DThreonine--tRNA ligase (EC 6.1.1.3)protein13831% helix, 41% strandQ58597
CThreonine--tRNA ligase (EC 6.1.1.3)protein13732% helix, 41% strandQ58597

Ligands and binding sites

  • A3T · 3'-deoxy-3'-(L-threonylamino)adenosine · ligand · 3 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1640.770.9914empty
22390.640.8227A3T
32250.630.8226A3T
42710.610.8030empty
52400.610.8029A3T

Interfaces

3 interfaces between chains.

  • C–D · 1158 Ų buried · 14 hydrogen bonds · protein-protein
  • A–B · 1104 Ų buried · 11 hydrogen bonds · protein-protein
  • B–C · 177 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 4RRG · Editing domain of threonyl-tRNA synthetase from methanococcus jannaschii with L-THR3AA · the same entry in another collection · chain D against D, TM-score 1.00
  • Q58597 · AlphaFold monomer V2.0 prediction for threonine--tRNA ligase (Q58597) · a predicted model of the same protein · chain B against A, TM-score 0.99

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