Affinage · Plasmodium

TOM7

PF3D7_0823700 · mitochondrial import receptor subunit TOM7, 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

PF3D7_0823700 (TOM7) is identified as a conserved core subunit of the translocase of the outer mitochondrial membrane (TOM complex) in Plasmodium falciparum, recognized by comparative sequence analysis as an ortholog present alongside Tom40 and Tom22 across diverse eukaryotes (PMID:15155803). Native complexomics places PF3D7_0823700 in co-migration with both the TOM complex and the ER membrane complex (EMC), raising the possibility that it bridges the ER and mitochondrion analogously to yeast TOM5, which is absent from the Plasmodium genome (PMID:39747010). Beyond its assignment as a TOM complex subunit and this co-migration observation, no direct functional characterization of PF3D7_0823700 has been performed in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 2 steps
  1. 2004 Low

    Before this work it was unclear whether Plasmodium encodes the small core TOM subunits; identifying a TOM7 ortholog established PF3D7_0823700 as a candidate conserved component of the mitochondrial protein import machinery.

    Evidence comparative sequence analysis / bioinformatic ortholog identification in P. falciparum

    PMID:15155803

    Open questions at the time
    • computational assignment only, with no functional experiment in Plasmodium
    • membership in an assembled TOM complex not demonstrated
    • no localization data for the protein itself
  2. 2025 Low

    To move beyond sequence prediction, native complexomics tested which complexes PF3D7_0823700 associates with, showing it co-migrates with both the TOM complex and the EMC and raising the hypothesis that it serves as an ER-mitochondrion tether in place of the absent yeast TOM5.

    Evidence native gel electrophoresis / complexomics co-migration with AlphaFold prediction and multiple sequence alignment in P. falciparum

    PMID:39747010

    Open questions at the time
    • single co-migration observation without direct functional validation of a tethering role
    • structural similarity to TOM5 is predicted, not experimentally confirmed
    • no genetic or biochemical test of ER-mitochondrion contact function

Open questions

Synthesis pass · forward-looking unresolved questions
  • Whether PF3D7_0823700 is functionally required for mitochondrial protein import and whether it physically tethers the ER to the mitochondrion remain untested.
  • no knockout/knockdown phenotype established
  • no reconstitution or interaction assay confirming the proposed EMC-mitochondrion bridge
  • import substrate dependence on PF3D7_0823700 not tested

Mechanism profile

Synthesis pass · controlled-vocabulary classification
Complex memberships
ER membrane complex (EMC) — co-migration onlyTOM complex (translocase of the outer mitochondrial membrane)

Evidence

Reading pass · 2 per-paper findings extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2004 Comparative sequence analysis identified a TOM7 ortholog in Plasmodium falciparum, suggesting it is a conserved core subunit of the translocase of the outer mitochondrial membrane (TOM complex), alongside Tom40 and Tom22, present across diverse eukaryotes. Comparative sequence analysis / bioinformatics identification of ortholog Molecular biology and evolution Low 15155803
2025 Native electrophoresis (complexomics) data showed that PfTOM7 (PF3D7_0823700) co-migrates with both the TOM complex and the ER membrane complex (EMC) in P. falciparum, suggesting PfTOM7 may serve as a tether bridging the ER and mitochondrion in a manner analogous to TOM5 in yeast, which is absent from the Plasmodium genome. Native gel electrophoresis / complexomics co-migration analysis; AlphaFold structural prediction and multiple sequence alignment Nature communications Low 39747010

Source papers

Stage 0 corpus · 3 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2004 Tom22', an 8-kDa trans-site receptor in plants and protozoans, is a conserved feature of the TOM complex that appeared early in the evolution of eukaryotes. Molecular biology and evolution 85 15155803
2025 Comparative 3D ultrastructure of Plasmodium falciparum gametocytes. Nature communications 0 39747010
2023 Protein KIC5 is a novel regulator of artemisinin stress response in the malaria parasite Plasmodium falciparum. Scientific reports 0 36624300