Affinage · Toxoplasma gondii

ICMAP3

intraconoidal microtubule-associated protein ICMAP3 · UniProt S8F519

Annotated
2026-09-08
1 papers in source corpus 1 papers cited in narrative 1 extracted findings

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

ICMAP3 is an intraconoidal microtubule-associated protein of Toxoplasma gondii that couples cytoskeletal organization at the apical complex to the secretory machinery required for host cell invasion. It functions through two distinct isoforms with separable roles: one contributes to the control of intraconoidal microtubule (ICMT) length, while the other mediates docking of two rhoptries at the apical vesicle, as revealed by conditional depletion causing loss of both functions (PMID:38191574). Beyond this depletion-based characterization (PMID:38191574), no further mechanistic detail — including binding partners, structural basis of isoform specialization, or the molecular mechanism of rhoptry docking — has been characterized in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2024 Medium

    It was unknown how intraconoidal microtubule length and rhoptry positioning at the apical vesicle are coordinated; depletion of ICMAP3 established that a single microtubule-associated protein, via two isoforms, governs both ICMT length control and rhoptry docking.

    Evidence Conditional protein depletion with ultrastructural and functional readouts of ICMT length and rhoptry docking at the apical vesicle in Toxoplasma gondii

    PMID:38191574

    Open questions at the time
    • The molecular basis by which the two isoforms partition between ICMT length control and rhoptry docking is not defined
    • No binding partners or structural interactions with microtubules or rhoptries are identified
    • The mechanism linking rhoptry docking to sustained discharge and invasion is not directly demonstrated

Open questions

Synthesis pass · forward-looking unresolved questions
  • How ICMAP3 isoforms physically associate with intraconoidal microtubules and the apical vesicle, and what partners mediate rhoptry docking, remain unresolved.
  • No interactome or reciprocal binding data
  • No structural model of ICMAP3 or its isoforms
  • Strain-level generality not addressed

Mechanism profile

Synthesis pass · controlled-vocabulary classification
No controlled-vocabulary terms were assigned to this entry.

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2024 ICMAP3 exists in two isoforms that contribute to the control of intraconoidal microtubule (ICMT) length and the docking of two rhoptries at the apical vesicle (AV), respectively, as demonstrated by depletion experiments showing loss of these functions. Conditional protein depletion (loss-of-function) with ultrastructural and functional readouts of ICMT length control and rhoptry docking at the apical vesicle Nature Communications Medium 38191574

Source papers

Stage 0 corpus · 1 paper · ranked by NIH iCite citations
Year Title Journal Citations PMID
2024 Sustained rhoptry docking and discharge requires Toxoplasma gondii intraconoidal microtubule-associated proteins. Nature communications 16 38191574