The Plasmodium falciparum Schizont Phosphoproteome Reveals Extensive Phosphatidylinositol and cAMP-Protein Kinase A Signaling

Dataset UNKNOWN
Lasonder, Edwin; Green, Judith L.; Camarda, Grazia; Talabani, Hana; Holder, Anthony A.; Langsley, Gordon; Alano, Pietro;
(2012)
  • Publisher: Figshare
  • Related identifiers: doi: 10.1021/pr300557m.s006, doi: 10.1021/pr300557m.s007, doi: 10.1021/pr300557m.s008, doi: 10.1021/pr300557m.s009, doi: 10.1021/pr300557m.s004, doi: 10.1021/pr300557m.s005
  • Subject: Molecular Biology | blood cell | Plasmodium falciparum cause | host cell invasion | falciparum schizonts | GAP 45 | protein kinases | CDPK 1 | phosphorylation sites | merozoite egress | phosphoprotein interaction network | inositol pathway | blood cell invasion | kinase assay | Genetics | Prominent roles | Extensive Phosphatidylinositol | implicating cAMP | parasite multiplication | Developmental Biology | glideosome motor | Microbiology | CDPK 1. | Medicine | analysis | SignalingThe asexual blood stages | Computational Biology | novel PKA substrates | Plasmodium falciparum Schizont Phosphoproteome | Cell Biology | 871 novel sites | Biochemistry | Cancer
    • FOR: 29999 Physical Sciences not elsewhere classified | 69999 Biological Sciences not elsewhere classified

The asexual blood stages of <i>Plasmodium falciparum</i> cause the most lethal form of human malaria. During growth within an infected red blood cell, parasite multiplication and formation of invasive merozoites is called schizogony. Here, we present a detai... View more
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