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Mapping PP1c and Its Inhibitor 2 Interactomes Reveals Conserved and Specific Networks in Asexual and Sexual Stages of Plasmodium

International journal of molecular sciences, 2022-02, Vol.23 (3), p.1069

2022

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Essential role of GEXP15, a specific Protein Phosphatase type 1 partner, in Plasmodium berghei in asexual erythrocytic proliferation and transmission

PLoS pathogens, 2019-07, Vol.15 (7), p.e1007973-e1007973

2019

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Analysis of the interactome of the Ser/Thr Protein Phosphatase type 1 in Plasmodium falciparum

BMC genomics, 2016-03, Vol.17 (246), p.246-246, Article 246

2016

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The Antimalarial Ferroquine: Role of the Metal and Intramolecular Hydrogen Bond in Activity and Resistance

ACS chemical biology, 2011-03, Vol.6 (3), p.275-287

2011

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Plasmodium pseudo-Tyrosine Kinase-like binds PP1 and SERA5 and is exported to host erythrocytes

Scientific reports, 2019-05, Vol.9 (1), p.8120, Article 8120

2019

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Differential Fractionation of Erythrocytes Infected by Plasmodium berghei

Bio-protocol, 2020-06, Vol.10 (11), p.e3647-e3647

2020

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Characterization of a Protein Phosphatase Type-1 and a Kinase Anchoring Protein in Plasmodium falciparum

Frontiers in microbiology, 2018-10, Vol.9, p.2617-2617

2018

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Deciphering the Role of Protein Phosphatases in Apicomplexa: The Future of Innovative Therapeutics?

Microorganisms (Basel), 2022-03, Vol.10 (3), p.585

2022

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Plasmodium berghei leucine-rich repeat protein 1 downregulates protein phosphatase 1 activity and is required for efficient oocyst development

Open biology, 2022-08, Vol.12 (8), p.220015-220015

2022

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Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins

Frontiers in microbiology, 2016-10, Vol.7 (1682), p.1682

2016

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Drug-induced exposure of Schistosoma mansoni antigens SmCD59a and SmKK7

PLoS neglected tropical diseases, 2015-03, Vol.9 (3), p.e0003593-e0003593

2015

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PhosphoTyrosyl phosphatase activator of Plasmodium falciparum: identification of its residues involved in binding to and activation of PP2A

International journal of molecular sciences, 2014-02, Vol.15 (2), p.2431-2453

2014

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Human IgG1 Responses to Surface Localised Schistosoma mansoni Ly6 Family Members Drop following Praziquantel Treatment

PLoS neglected tropical diseases, 2015, Vol.9 (7), p.e0003920-e0003920

2015

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Inhibition of protein-protein interactions in Plasmodium falciparum: future drug targets

Current pharmaceutical design, 2012, Vol.18 (24), p.3522

2012

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Phosphatases are emerging as novel druggable targets in Plasmodium

Future microbiology, 2016-05, Vol.11 (5), p.603-606

2016

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A potent HDAC inhibitor blocks Toxoplasma gondii tachyzoite growth and profoundly disrupts parasite gene expression

International journal of antimicrobial agents, 2022-03, Vol.59 (3), p.106526-106526, Article 106526

2022

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Hydroxamate-based compounds are potent inhibitors of Toxoplasma gondii HDAC biological activity

Antimicrobial agents and chemotherapy, 2023-11, Vol.67 (11), p.e0066123-e0066123

2023

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Phosphatases are emerging as novel druggable targets in

Future microbiology, 2016-05, Vol.11 (5), p.603-606

2016

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Regulation of protein phosphatase type 1 and cell cycle progression by PfLRR1, a novel leucine‐rich repeat protein of the human malaria parasite Plasmodium falciparum

Molecular microbiology, 2006-05, Vol.60 (3), p.578-590

2006

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The Multifaceted Role of Protein Phosphatase 1 in Plasmodium

Trends in parasitology, 2021-02, Vol.37 (2), p.154-164

2021

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Identification of a Novel Antigen of Schistosoma mansoni Shared with Plasmodium falciparum and Evaluation of Different Cross-Reactive Antibody Subclasses Induced by Human Schistosomiasis and Malaria

Infection and Immunity, 2006-06, Vol.74 (6), p.3347-3354

2006

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International Journal of Antimicrobial Agents A potent HDAC inhibitor blocks Toxoplasma gondii tachyzoite growth and profoundly disrupts parasite gene expression

International journal of antimicrobial agents, 2022

2022

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The Drosophila melanogaster antimicrobial peptides Mtk-1 and Mtk-2 are active against the malarial parasite Plasmodium falciparum

Parasitology research (1987), 2019-06, Vol.118 (6), p.1993-1998

2019

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Identification of novel quinazoline derivatives as potent antiplasmodial agents

European journal of medicinal chemistry, 2019-01, Vol.161, p.277-291

2019

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Genome wide in silico analysis of Plasmodium falciparum phosphatome

BMC genomics, 2014-11, Vol.15 (1), p.1024-1024, Article 1024

2014

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Mapping PP1c and Its Inhibitor 2 Interactomes Reveals Conserved and Specific Networks in Asexual and Sexual Stages of Plasmodium

Essential role of GEXP15, a specific Protein Phosphatase type 1 partner, in Plasmodium berghei in asexual erythrocytic proliferation and transmission

Analysis of the interactome of the Ser/Thr Protein Phosphatase type 1 in Plasmodium falciparum

The Antimalarial Ferroquine: Role of the Metal and Intramolecular Hydrogen Bond in Activity and Resistance

Plasmodium pseudo-Tyrosine Kinase-like binds PP1 and SERA5 and is exported to host erythrocytes

Differential Fractionation of Erythrocytes Infected by Plasmodium berghei

Characterization of a Protein Phosphatase Type-1 and a Kinase Anchoring Protein in Plasmodium falciparum

Deciphering the Role of Protein Phosphatases in Apicomplexa: The Future of Innovative Therapeutics?

Plasmodium berghei leucine-rich repeat protein 1 downregulates protein phosphatase 1 activity and is required for efficient oocyst development

Antiplasmodial Activity Is an Ancient and Conserved Feature of Tick Defensins

Drug-induced exposure of Schistosoma mansoni antigens SmCD59a and SmKK7

PhosphoTyrosyl phosphatase activator of Plasmodium falciparum: identification of its residues involved in binding to and activation of PP2A

Human IgG1 Responses to Surface Localised Schistosoma mansoni Ly6 Family Members Drop following Praziquantel Treatment

Inhibition of protein-protein interactions in Plasmodium falciparum: future drug targets

Phosphatases are emerging as novel druggable targets in Plasmodium

A potent HDAC inhibitor blocks Toxoplasma gondii tachyzoite growth and profoundly disrupts parasite gene expression

Hydroxamate-based compounds are potent inhibitors of Toxoplasma gondii HDAC biological activity

Phosphatases are emerging as novel druggable targets in

Regulation of protein phosphatase type 1 and cell cycle progression by PfLRR1, a novel leucine‐rich repeat protein of the human malaria parasite Plasmodium falciparum

The Multifaceted Role of Protein Phosphatase 1 in Plasmodium

Identification of a Novel Antigen of Schistosoma mansoni Shared with Plasmodium falciparum and Evaluation of Different Cross-Reactive Antibody Subclasses Induced by Human Schistosomiasis and Malaria

International Journal of Antimicrobial Agents A potent HDAC inhibitor blocks Toxoplasma gondii tachyzoite growth and profoundly disrupts parasite gene expression

The Drosophila melanogaster antimicrobial peptides Mtk-1 and Mtk-2 are active against the malarial parasite Plasmodium falciparum

Identification of novel quinazoline derivatives as potent antiplasmodial agents

Genome wide in silico analysis of Plasmodium falciparum phosphatome

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