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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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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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Phosphatases are emerging as novel druggable targets in

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

2016

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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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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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Differential Fractionation of Erythrocytes Infected by Plasmodium berghei

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

2020

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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

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

Phosphatases are emerging as novel druggable targets in

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

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

Differential Fractionation of Erythrocytes Infected by Plasmodium berghei

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