Structural Insights into the <i>Giardia lamblia</i> Target of Rapamycin Homolog: A Bioinformatics Approach

TOR proteins, also known as targets of rapamycin, are serine/threonine kinases involved in various signaling pathways that regulate cell growth. The protozoan parasite <i>Giardia lamblia</i> is the causative agent of giardiasis, a neglected infectious disease in humans. In this study, we...

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Bibliographic Details
Main Authors: Patricia L. A. Muñoz-Muñoz, Rosa E. Mares-Alejandre, Samuel G. Meléndez-López, Marco A. Ramos-Ibarra
Format: Article
Language:English
Published: MDPI AG 2023-07-01
Series:International Journal of Molecular Sciences
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Online Access:https://www.mdpi.com/1422-0067/24/15/11992
Description
Summary:TOR proteins, also known as targets of rapamycin, are serine/threonine kinases involved in various signaling pathways that regulate cell growth. The protozoan parasite <i>Giardia lamblia</i> is the causative agent of giardiasis, a neglected infectious disease in humans. In this study, we used a bioinformatics approach to examine the structural features of GTOR, a <i>G. lamblia</i> TOR-like protein, and predict functional associations. Our findings confirmed that it shares significant similarities with functional TOR kinases, including a binding domain for the FKBP-rapamycin complex and a kinase domain resembling that of phosphatidylinositol 3-kinase-related kinases. In addition, it can form multiprotein complexes such as TORC1 and TORC2. These results provide valuable insights into the structure–function relationship of GTOR, highlighting its potential as a molecular target for controlling <i>G. lamblia</i> cell proliferation. Furthermore, our study represents a step toward rational drug design for specific anti-giardiasis therapeutic agents.
ISSN:1661-6596
1422-0067