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Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression

The urgent requirement of next generation antimalarials has been of recent interest due to the emergence of drug-resistant parasite. The genome-wide analysis of Plasmodium falciparum helicases revealed three RuvB proteins. Due to the presence of helicase motif I and II in PfRuvBs, there is a high pr...

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Autores principales: Ahmad, Moaz, Tuteja, Renu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460840/
https://www.ncbi.nlm.nih.gov/pubmed/23060959
http://dx.doi.org/10.4161/cib.20005
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author Ahmad, Moaz
Tuteja, Renu
author_facet Ahmad, Moaz
Tuteja, Renu
author_sort Ahmad, Moaz
collection PubMed
description The urgent requirement of next generation antimalarials has been of recent interest due to the emergence of drug-resistant parasite. The genome-wide analysis of Plasmodium falciparum helicases revealed three RuvB proteins. Due to the presence of helicase motif I and II in PfRuvBs, there is a high probability that they contain ATPase and possibly helicase activity. The Plasmodium database has homologs of several key proteins that interact with RuvBs and are most likely involved in the cell cycle progression, chromatin remodeling, and other cellular activities. Phylogenetically PfRuvBs are closely related to Saccharomyces cerevisiae RuvB, which is essential for cell cycle progression and survival of yeast. Thus PfRuvBs can serve as potential drug target if they show an essential role in the survival of parasite.
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spelling pubmed-34608402012-10-11 Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression Ahmad, Moaz Tuteja, Renu Commun Integr Biol Review The urgent requirement of next generation antimalarials has been of recent interest due to the emergence of drug-resistant parasite. The genome-wide analysis of Plasmodium falciparum helicases revealed three RuvB proteins. Due to the presence of helicase motif I and II in PfRuvBs, there is a high probability that they contain ATPase and possibly helicase activity. The Plasmodium database has homologs of several key proteins that interact with RuvBs and are most likely involved in the cell cycle progression, chromatin remodeling, and other cellular activities. Phylogenetically PfRuvBs are closely related to Saccharomyces cerevisiae RuvB, which is essential for cell cycle progression and survival of yeast. Thus PfRuvBs can serve as potential drug target if they show an essential role in the survival of parasite. Landes Bioscience 2012-07-01 /pmc/articles/PMC3460840/ /pubmed/23060959 http://dx.doi.org/10.4161/cib.20005 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Ahmad, Moaz
Tuteja, Renu
Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression
title Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression
title_full Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression
title_fullStr Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression
title_full_unstemmed Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression
title_short Plasmodium falciparum RuvB proteins: Emerging importance and expectations beyond cell cycle progression
title_sort plasmodium falciparum ruvb proteins: emerging importance and expectations beyond cell cycle progression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460840/
https://www.ncbi.nlm.nih.gov/pubmed/23060959
http://dx.doi.org/10.4161/cib.20005
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