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Crystal structure of lysyl-tRNA synthetase from plasmodium falciparum complexed with L-lysine and clado-B

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
6L4Q
Type
protein
Length
972 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lysine--tRNA ligase
EC
6.1.1.6
UniProt
Q8IDJ8
Ligands
E5R, LYS
Pockets
12 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 29% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BLysine--tRNA ligase (EC 6.1.1.6)protein48531% helix, 25% strandQ8IDJ8
ALysine--tRNA ligase (EC 6.1.1.6)protein48727% helix, 25% strandQ8IDJ8

Ligands and binding sites

  • E5R · (3R)-3-[[(3R)-3-methylpiperidin-1-yl]methyl]-6,8-bis(oxidanyl)-3,4-dihydroisochromen-1-one · ligand · 2 copies · chains B, A
  • LYS · Lysine · ligand · 2 copies · chains B, A

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

Pockets

12 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13770.780.8772empty
26280.750.8268E5R, LYS
36760.750.8160E5R, LYS
42370.710.8627empty
52760.700.8437empty

Interfaces

1 interface between chains.

  • B–A · 4620 Ų buried · 57 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6L4Q · Crystal Structure of Lysyl-tRNA Synthetase from Plasmodium falciparum complexed with… · the same entry in another collection · chain B against B, TM-score 1.00

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