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TitleStructural Plasticity of Plasmodium falciparum Plasmepsin X to Accommodate Binding of Potent Macrocyclic Hydroxyethylamine Inhibitors.
Journal, issue, pagesJ. Mol. Biol., Vol. 437, Page 169062-169062, Year 2025
Publish dateNov 5, 2024 (structure data deposition date)
AuthorsWithers-Martinez, C. / George, R. / Ogrodowicz, R. / Kunzelmann, S. / Purkiss, A.G. / Kjaer, S. / Walker, P.A. / Kovada, V. / Jirgensons, A. / Blackman, M.J.
External linksJ. Mol. Biol. / PubMed:40043835
MethodsX-ray diffraction
Resolution1.7 Å
Structure data

PDB-9hb0:
Crystal structure of Plasmodium falciparum Plasmepsin X in complex with the hydroxyethylamine drug 7k.
Method: X-RAY DIFFRACTION / Resolution: 1.7 Å

Chemicals

PDB-1itu:
HUMAN RENAL DIPEPTIDASE COMPLEXED WITH CILASTATIN

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

Source
  • plasmodium falciparum 3d7 (eukaryote)
KeywordsHYDROLASE / Aspartyl protease / hydroxyethylamine inhibitor / complex / non-covalent.

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