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Trypanosoma brucei methionyl-tRNA synthetase in complex with inhibitor 1-{3-[(5-chloro-2-hydroxy-3-IODOBENZYL)AMINO]PROPYL}-3-thiophen-3- ylurea (chem 1473)

Analyse Trypanosoma brucei methionyl-tRNA synthetase in complex with inhibitor… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4MW4
Type
protein
Length
1,056 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Methionyl-tRNA synthetase
EC
6.1.1.10
UniProt
Q38C91
Ligands
MET, 2EB, SO4
Pockets
15 · best druggability 0.76

Structure

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

ChainMoleculeTypeResiduesSecondary structureUniProt
AMethionyl-tRNA synthetase (EC 6.1.1.10)protein52350% helix, 17% strandQ38C91
BMethionyl-tRNA synthetase (EC 6.1.1.10)protein53349% helix, 18% strandQ38C91

Ligands and binding sites

  • MET · Methionine · ligand · chains A
  • 2EB · 1-{3-[(5-chloro-2-hydroxy-3-iodobenzyl)amino]propyl}-3-thiophen-3-ylurea · ligand · chains B
  • SO4 · Sulfate ion · ion · 3 copies · chains A, B
  • GOL · Glycerol · additive · 9 copies · chains A, B
  • DMS · Dimethyl sulfoxide · additive · 5 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15510.760.8350empty
25700.690.7866GOL, DMS, SO4, 2EB
34440.670.7954DMS, MET
41300.440.7628empty
51270.410.7513empty

Interfaces

1 interface between chains.

  • A–B · 1483 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 modified (artifact).

Compared structures

  • 4MW4 · Trypanosoma brucei methionyl-tRNA synthetase in complex with inhibitor… · the same entry in another collection · chain A against A, TM-score 1.00

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