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TitleChemoproteomics validates selective targeting of Plasmodium M1 alanyl aminopeptidase as an antimalarial strategy.
Journal, issue, pagesElife, Vol. 13, Year 2024
Publish dateApr 24, 2023 (structure data deposition date)
AuthorsGiannangelo, C. / Challis, M.P. / Siddiqui, G. / Edgar, R. / Malcolm, T.R. / Webb, C.T. / Drinkwater, N. / Vinh, N. / Macraild, C. / Counihan, N. ...Giannangelo, C. / Challis, M.P. / Siddiqui, G. / Edgar, R. / Malcolm, T.R. / Webb, C.T. / Drinkwater, N. / Vinh, N. / Macraild, C. / Counihan, N. / Duffy, S. / Wittlin, S. / Devine, S.M. / Avery, V.M. / De Koning-Ward, T. / Scammells, P. / McGowan, S. / Creek, D.J.
External linksElife / PubMed:38976500
MethodsX-ray diffraction
Resolution1.55 Å
Structure data

PDB-8slo:
Plasmodium falciparum M1 aminopeptidase bound to selective inhibitor MIPS2673
Method: X-RAY DIFFRACTION / Resolution: 1.55 Å

Chemicals

ChemComp-ZN:
Unknown entry


ChemComp, No image

ChemComp-BYW:
Unknown entry

ChemComp-MG:
Unknown entry

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

Source
  • plasmodium falciparum (malaria parasite P. falciparum)
KeywordsHYDROLASE/HYDROLASE inhibitor / Plasmodium falciparum / malaria / metallo-exopeptidase / M1 aminopeptidase / aminopeptidase / HYDROLASE / HYDROLASE-HYDROLASE inhibitor complex

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