Affinage · Plasmodium

MED10

PF3D7_0707600 · mediator of RNA polymerase II transcription subunit 10, putative

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

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

PF3D7_0707600 (MED10) is a putative subunit of the Mediator complex in Plasmodium falciparum, identified through co-immunoprecipitation of the conserved Mediator subunit PfMed31 followed by mass spectrometry in blood-stage parasites (PMID:35557691). This finding places MED10 within the parasite Mediator complex via its association with PfMed31 (PMID:35557691). Beyond this complex-membership assignment, no specific enzymatic activity, structural role, or individual function of MED10 has been characterized in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2022 Medium

    Whether P. falciparum possesses a MED10 subunit associated with its Mediator complex was unknown; identifying MED10 as a PfMed31 interaction partner established its membership in the parasite Mediator complex.

    Evidence Co-immunoprecipitation of tagged PfMed31 followed by mass spectrometric identification in blood-stage P. falciparum parasites

    PMID:35557691

    Open questions at the time
    • Interaction inferred from a single co-IP/MS experiment in one lab without reciprocal validation from MED10's side
    • No individual molecular function, enzymatic activity, or structural role of MED10 established
    • No data on MED10 localization, essentiality, or stage-specific behavior within the parasite

Open questions

Synthesis pass · forward-looking unresolved questions
  • The specific function of MED10 within the P. falciparum Mediator complex, its target genes, and its role in RNA polymerase II transcription remain uncharacterized.
  • No functional or genetic characterization of MED10 beyond complex membership
  • No structural model of MED10 or its interface within the Mediator complex
  • No evidence linking MED10 to specific transcriptional programs or parasite phenotypes

Mechanism profile

Synthesis pass · controlled-vocabulary classification
Partners
Complex memberships
Mediator complex (P. falciparum)

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2022 PF3D7_0707600 (MED10/PfMed10) was identified as a co-immunoprecipitated interaction partner of the conserved Mediator subunit PfMed31, placing MED10 within the P. falciparum Mediator complex. This is consistent with known yeast two-hybrid, co-IP, and structural data in other organisms showing Med31 specifically interacts with Med10. Coimmunoprecipitation of tagged PfMed31 followed by mass spectrometric analysis in blood-stage P. falciparum parasites ACS omega Medium 35557691

Source papers

Stage 0 corpus · 2 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2019 Protein-RNA interactions important for Plasmodium transmission. PLoS pathogens 16 31877193
2022 Mediator Complex of the Malaria Parasite Plasmodium falciparum Associates with Evolutionarily Novel Subunits. ACS omega 0 35557691