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Crystal Structure of Lysyl-tRNA Synthetase from Plasmodium falciparum complexed with L-lysine and Clado-C

Analyse Crystal Structure of Lysyl-tRNA Synthetase from Plasmodium falciparum complexed… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6L3Y
Type
protein
Length
966 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
3.1
Source
Plasmodium falciparum 3D7
Molecule
Lysine--tRNA ligase
EC
6.1.1.6
UniProt
Q8IDJ8
Ligands
LYS, E5C, PO4
Pockets
14 · best druggability 0.81

Structure

x-ray diffraction · resolution 3.1 · 2 distinct chains · 30% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BLysine--tRNA ligase (EC 6.1.1.6)protein48430% helix, 26% strandQ8IDJ8
ALysine--tRNA ligase (EC 6.1.1.6)protein48230% helix, 26% strandQ8IDJ8

Ligands and binding sites

  • LYS · Lysine · ligand · 2 copies · chains B, A
  • E5C · (3R)-3-[[(3S)-3-ethylpiperidin-1-yl]methyl]-6,8-bis(oxidanyl)-3,4-dihydroisochromen-1-one · ligand · 2 copies · chains B, A
  • PO4 · Phosphate ion · ion · 5 copies · chains B, A

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

Pockets

14 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11560.810.9740empty
27200.760.8168LYS, E5C, PO4
37020.750.8158LYS, E5C, PO4
42510.740.8834empty
52750.720.8637empty

Interfaces

1 interface between chains.

  • B–A · 4673 Ų buried · 64 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6L3Y · Crystal structure of lysyl-tRNA synthetase from plasmodium falciparum complexed with… · the same entry in another collection · chain A against A, TM-score 1.00

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