Affinage · Plasmodium

TOC75

PF3D7_1234600 · protein TOC75, putative

Annotated
2026-09-08
3 papers in source corpus 2 papers cited in narrative 2 extracted findings

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

TOC75 (PF3D7_1234600) is an Omp85-family protein encoded in the Plasmodium falciparum genome that has been assigned, on evolutionary grounds, as the candidate pore-forming component of the Translocon of the Outer Chloroplast membrane (TOC) at an inner membrane of the apicoplast, a role inferred from electrophysiological characterization of the related diatom Omp85 homolog rather than from direct study of the Plasmodium protein (PMID:20042599). It has additionally been listed among the small set of putative TOC/TIC translocon components involved in apicoplast protein import (PMID:22144892). Beyond this evolutionary assignment and its citation as a mutant-validated import factor, no direct in vitro, biochemical, or structural characterization of TOC75 itself has been reported in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 2 steps
  1. 2009 Low

    To identify the machinery importing nuclear-encoded proteins across apicoplast membranes, TOC75 was recognized as an apicomplexan Omp85-family protein and assigned a pore-forming TOC role, establishing the first mechanistic hypothesis for the protein.

    Evidence Bioinformatic identification and evolutionary comparison in P. falciparum, with function inferred from electrophysiology of the diatom Omp85 ortholog

    PMID:20042599

    Open questions at the time
    • Function inferred computationally and by analogy to the diatom ortholog; no direct experiment performed on the Plasmodium TOC75 protein
    • No demonstration that PF3D7_1234600 forms a channel or resides in the proposed membrane
    • No structural model of the Plasmodium protein
  2. 2011 Low

    To place TOC75 within the apicoplast import apparatus, it was cataloged among the putative TOC/TIC translocon components and cited as having a mutant-validated import role, reinforcing its assignment to the import machinery.

    Evidence Systematic bioinformatic screen with epitope-tagging and conditional mutant analysis of apicoplast proteins in P. falciparum; TOC75 role cited as prior work

    PMID:22144892

    Open questions at the time
    • Mutant validation of TOC75 is cited as prior work rather than directly demonstrated, with no full experimental detail for TOC75 itself
    • Membership in the translocon is asserted without direct interaction data for PF3D7_1234600
    • No biochemical evidence linking TOC75 loss to failed protein import

Open questions

Synthesis pass · forward-looking unresolved questions
  • Whether PF3D7_1234600 itself forms a translocation pore, its precise membrane localization, its interaction partners within a TOC/TIC complex, and its substrate spectrum remain unestablished by direct experiment.
  • No channel/reconstitution assay on the Plasmodium protein
  • No structural data
  • No direct demonstration of complex membership or import substrates for PF3D7_1234600

Mechanism profile

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

Evidence

Reading pass · 2 per-paper findings extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2009 TOC75 (PF3D7_1234600) was identified as an Omp85-family protein encoded in apicomplexan (Plasmodium falciparum) genomes, proposed to function as the pore-forming component of the Translocon of the Outer Chloroplast membrane (TOC) at the outermost inner membrane of the apicoplast, based on evolutionary and electrophysiological analysis of the related diatom Omp85 homolog. Bioinformatic identification and evolutionary comparison; electrophysiological characterization of the diatom ortholog used to infer function of the Plasmodium homolog The Journal of biological chemistry Low 20042599
2011 TOC75 (PF3D7_1234600) was identified as one of a small number of putative components of the TOC/TIC translocon complexes in apicomplexans, with its critical role in apicoplast protein import validated through mutant analysis (as referenced in the context of the broader apicoplast import machinery description). Systematic bioinformatic screen combined with experimental epitope-tagging and conditional mutant analysis (promoter replacement strategy) for apicoplast proteins; TOC75 cited as having mutant-validated import role PLoS pathogens Low 22144892

Source papers

Stage 0 corpus · 3 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2009 Filling the gap, evolutionarily conserved Omp85 in plastids of chromalveolates. The Journal of biological chemistry 60 20042599
2020 Directing traffic: Chaperone-mediated protein transport in malaria parasites. Cellular microbiology 0 32388921
2011 A systematic screen to discover and analyze apicoplast proteins identifies a conserved and essential protein import factor. PLoS pathogens 0 22144892