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Parasitologists United Journal
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Volume Volume 18 (2025)
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Abaza, S. (2022). Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part II: Parasite targets. Parasitologists United Journal, 15(1), 22-38. doi: 10.21608/PUJ.2022.129311.1160
Sherif Abaza. "Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part II: Parasite targets". Parasitologists United Journal, 15, 1, 2022, 22-38. doi: 10.21608/PUJ.2022.129311.1160
Abaza, S. (2022). 'Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part II: Parasite targets', Parasitologists United Journal, 15(1), pp. 22-38. doi: 10.21608/PUJ.2022.129311.1160
Abaza, S. Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part II: Parasite targets. Parasitologists United Journal, 2022; 15(1): 22-38. doi: 10.21608/PUJ.2022.129311.1160

Recent advances in identification of potential drug targets and development of novel drugs in parasitic diseases. Part II: Parasite targets

Article 3, Volume 15, Issue 1, April 2022, Page 22-38  XML PDF (505.14 K)
Document Type: Review Article
DOI: 10.21608/PUJ.2022.129311.1160
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Author
Sherif Abaza email
Medical Parasitology Department, Faculty of Medicine, Suez Canal University, Ismailia, Egypt
Abstract
Understanding the parasite biology on molecular basis is the starting point for identification of novel parasite
drug targets. The interpretation of gene regulatory networks is a “blueprint” for discovery of new interactions
among system biological events that lead to identification of novel potential drug targets and/or vaccine
candidates. The aim of the present review is to simplify the molecular bases of the mandatory biological
processes involved in the parasite survival, growth, replication, pathogenesis, and virulence. Growth and
replication include nucleic acid synthesis, DNA replication and gene expression (topoisomerase, histone
variants, and histone modification enzymes), and translation process for protein synthesis (initiation and
elongation factors). Parasite survival includes signaling pathways (protein kinases, and protein lipidadtion),
regulated cell death machinery, mitochondrial respiratory electron chain, and transmembrane transporters.
Parasite pathogenesis and virulence include proteases, endogenous protease inhibitors (cysteine and serine
protease inhibitors), heat shock proteins, glycoproteins, and tetraspanins. This publication is part II in a series
of reviews dealing with identification of potential drug targets and development of novel drugs in parasitic
diseases published in PUJ as part I[1].
Keywords
cytochrome complex; myristoylation; protein kinases; proteases; regulated cell death; salvage pathway; sirtuins; topoisomerase; transporters
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