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Crystal structure of T. cruzi histidyl-tRNA synthetase in complex with 2-aminoquinolin-8-ol (chem 89)

Analyse Crystal structure of T. cruzi histidyl-tRNA synthetase in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4YRC
Type
protein
Length
419 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Histidyl-tRNA synthetase
EC
6.1.1.21
UniProt
Q4DA54
Ligands
0P6, HIS, SO4
Pockets
3 · best druggability 0.73

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHistidyl-tRNA synthetase (EC 6.1.1.21)protein41942% helix, 20% strandQ4DA54

Ligands and binding sites

  • 0P6 · 2-aminoquinolin-8-ol · ligand · 2 copies · chains A
  • HIS · Histidine · ligand · chains A
  • SO4 · Sulfate ion · ion · 2 copies · chains A
  • DMS · Dimethyl sulfoxide · additive · 3 copies · chains A
  • EDO · 1,2-ethanediol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16190.730.8157HIS, 0P6
21140.420.7621empty
31190.390.7522DMS

Compared structures

  • 4YRC · Crystal structure of T. cruzi Histidyl-tRNA synthetase in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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