Global kinomic and phospho-proteomic analyses of the human malaria parasite Plasmodium falciparum

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PDF) Global kinomic and phospho-proteomic analyses of the human malaria parasite Plasmodium falciparum

Global analysis of putative phospholipases in the malaria parasite Plasmodium falciparum reveals critical factors for parasite proliferation

Inducing controlled cell cycle arrest and re-entry during asexual

Protein kinase PfPK2 mediated signalling is critical for host erythrocyte invasion by malaria parasite

A divergent cyclin/cyclin-dependent kinase complex controls the

Comparative analysis of the kinomes of Plasmodium falciparum, Plasmodium vivax and their host Homo sapiens, BMC Genomics

Phosphoproteomics reveals malaria parasite Protein Kinase G as a signalling hub regulating egress and invasion

PDF) A new tool for the chemical genetic investigation of the

Comparative analysis of the kinomes of Plasmodium falciparum, Plasmodium vivax and their host Homo sapiens, BMC Genomics

The Plasmodium falciparum schizont phosphoproteome reveals extensive phosphatidylinositol and cAMP-protein kinase A signaling.

An ancient protein phosphatase, SHLP1, is critical to microneme

Co-option of Plasmodium falciparum PP1 for egress from host erythrocytes. - Abstract - Europe PMC

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Protein Modification Characteristics of the Malaria Parasite