Target intelligence / Profile preview

Parasite microtubule

Molecular classification
Cytoskeletal protein, Other
01

Overview

Parasite microtubules are cytoskeletal filaments of tubulin that play crucial roles in maintaining parasite cell morphology, enabling cell division, host cell invasion, intracellular trafficking, and motility such as flagellar movement[1][2][3][5][7]. While tubulin is highly conserved, subtle structural differences in parasite microtubules, especially in the drug-binding sites, allow for selective targeting by antiparasitic drugs without harming host microtubules[2][6][8]. These structures are especially prominent in forms such as subpellicular microtubule arrays (defining parasite shape and rigidity), axonemal microtubules (flagellar movement), and specialized assemblies like the conoid (invasion machinery)[1][3][5][7]. Drug classes such as dinitroanilines and benzimidazoles inhibit parasite microtubule formation and function, representing proven and promising antiparasitic strategies[2][6][8]. Parasite microtubules remain a focus for combating major parasitic infections, although challenges such as resistance and selectivity persist.

Other names
Subpellicular microtubuleCortical microtubuleAxonemal microtubule*Plasmodium* microtubule*Toxoplasma* microtubule*Trypanosoma* microtubuleKinetoplastid microtubuleSPMT/subpellicular microtubule
02

Mechanism of action

Inhibition of microtubule polymerization (preventing tubulin assembly)\nDisruption of microtubule function, leading to impaired parasite replication, host cell invasion, and morphology

03

Biological functions

Maintenance of cell shapeCell division (cytokinesis)Host cell invasionMotility/flagellar functionMorphogenesis
04

Disease associations

Infection (malaria, leishmaniasis, trypanosomiasis, toxoplasmosis and other parasitic diseases)
05

Safety considerations

Host toxicity: risk of cross-reactivity with host (human) microtubules, but parasite microtubules offer structural differences that can be exploited for selectivityDrug resistance: rapid emergence of resistance is a notable challengeEssentiality: targeting an essential cytoskeletal component may cause broad effects
06

Interacting drugs

Parabulin

3 more in the full profile.

07

Biomarkers

Tubulin isoform expression levels (such as α- and β-tubulin in parasite species)Detection of microtubule-associated proteins (e.g., SPM1, TrxL1, FAP20, FAP52 in *Plasmodium*)

Beyond the preview

Go deeper on Parasite microtubule.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Drug pipeline

Full profile access

Explore the programs pursuing this target and their development progress.

  • Drug candidates
  • Developers
  • Development stage

Clinical trials

Full profile access

Follow the clinical studies evaluating therapies directed at this target.

  • Trial design
  • Status
  • Readouts

Competitive landscape

Full profile access

Compare approaches across drug candidates, modalities, and indications.

  • Programs
  • Modalities
  • Indications

Literature & evidence

Full profile access

Investigate the research and source evidence behind target biology and development.

  • Publications
  • Sources
  • Analysis

Patents

Full profile access

Explore patent activity around therapies and technologies addressing this target.

  • Patents
  • Assignees
  • Technologies

Research & analysis

Full profile access

Connect target biology, drug development, and emerging evidence in your research.

  • Biology
  • Development news
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on Parasite microtubule.

Explore the full profile

Gosset Free

Get started with Gosset.

Enter your work email and we’ll be in touch with next steps.

Work email preferred.

Book a call