Preliminary Structural Studies of the Kinetoplastida Target Enzyme and Foundation for Subsequent Studies

Kinetoplastida, a class of flagellated protists, includes several pathogenic genera responsible for neglected tropical diseases. These parasites rely on unique biochemical pathways, such as those involved in glycolysis, which are absent in their human hosts, making them attractive targets for selective drug development. This study presents a preliminary structural and functional analysis of a key target enzyme from Kinetoplastida, laying the foundation for further mechanistic studies and drug screening. Using a combination of homology modeling, molecular docking, and sequence alignment, we identify conserved active site residues and potential ligand binding regions. The results provide valuable insights for future structure-based drug design efforts aimed at treating Trypanosoma and Leishmania infections.

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Publication Details

Journal
European Journal of Public Health and Environmental Research
Published
2025-05-03
DOI
https://doi.org/10.71222/xwzr0q07
Primary Topic
Microtubule and mitosis dynamics
Type
article
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article

Preliminary Structural Studies of the Kinetoplastida Target Enzyme and Foundation for Subsequent Studies

Zhengzhe Liu
European Journal of Public Health and Environmental Research
Microtubule and mitosis dynamics
article

Preliminary Structural Studies of the Kinetoplastida Target Enzyme and Foundation for Subsequent Studies

Zhengzhe Liu
article en

Abstract

Kinetoplastida, a class of flagellated protists, includes several pathogenic genera responsible for neglected tropical diseases. These parasites rely on unique biochemical pathways, such as those involved in glycolysis, which are absent in their human hosts, making them attractive targets for selective drug development. This study presents a preliminary structural and functional analysis of a key target enzyme from Kinetoplastida, laying the foundation for further mechanistic studies and drug screening. Using a combination of homology modeling, molecular docking, and sequence alignment, we identify conserved active site residues and potential ligand binding regions. The results provide valuable insights for future structure-based drug design efforts aimed at treating Trypanosoma and Leishmania infections.

European Journal of Public Health and Environmental ResearchVol. 1(1)
University of Edinburgh (GB)
Openalex Percentile: Top 83%
Microtubule and mitosis dynamics
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