Ontology highlight
ABSTRACT:
INSTRUMENT(S): Q Exactive
ORGANISM(S): Plasmodium Falciparum (isolate 3d7)
TISSUE(S): Blood Cell
DISEASE(S): Malaria
SUBMITTER: Catherine Merrick
LAB HEAD: Catherine J Merrick
PROVIDER: PXD028903 | Pride | 2022-04-04
REPOSITORIES: Pride
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P834_3D7_GBP2_2.raw.raw | Raw | |||
P932_3D7_GBP2_1.raw.raw | Raw | |||
P932_3D7_WT_1.raw.raw | Raw | |||
allPeptides.txt | Txt | |||
checksum.txt | Txt |
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Edwards-Smallbone James J Jensen Anders L AL Roberts Lydia E LE Totañes Francis Isidore G FIG Hart Sarah R SR Merrick Catherine J CJ
Frontiers in cellular and infection microbiology 20220222
In the early-diverging protozoan parasite <i>Plasmodium</i>, few telomere-binding proteins have been identified and several are unique. <i>Plasmodium</i> telomeres, like those of most eukaryotes, contain guanine-rich repeats that can form G-quadruplex structures. In model systems, quadruplex-binding drugs can disrupt telomere maintenance and some quadruplex-binding drugs are potent anti-plasmodial agents. Therefore, telomere-interacting and quadruplex-interacting proteins may offer new targets f ...[more]