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Crystal structure of the 1-acyl-sn-glycerophosphate (lpa) acyltransferase, plsc, from thermotoga maritima

Analyse Crystal structure of the 1-acyl-sn-glycerophosphate (lpa) acyltransferase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5KYM
Type
protein
Length
473 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
1-acyl-sn-glycerol-3-phosphate acyltransferase
EC
2.3.1.51
UniProt
R4NS39
Ligands
HGX
Pockets
5 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 50% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A1-acyl-sn-glycerol-3-phosphate acyltransferase (EC 2.3.1.51)protein24150% helix, 12% strandR4NS39
B1-acyl-sn-glycerol-3-phosphate acyltransferase (EC 2.3.1.51)protein23249% helix, 11% strandR4NS39

Ligands and binding sites

  • HGX · 1-heptadecanoyl-2-tridecanoyl-3-glycerol-phosphonyl choline · ligand · 6 copies · chains A, B
  • DD9 · nonane · additive · 2 copies · chains A, B
  • LMT · Dodecyl-beta-D-maltoside · additive · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17080.770.8156DD9
26410.740.8057DD9
31420.420.7527empty
41440.410.7318empty
51440.390.7325empty

Interfaces

1 interface between chains.

  • A–B · 156 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5KYM · Crystal Structure of the 1-acyl-sn-glycerophosphate (LPA) acyltransferase, PlsC, from… · the same entry in another collection · chain A against A, TM-score 1.00

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