Affinage · Plasmodium

PTB

PF3D7_0606500 · polypyrimidine tract-binding protein, 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_0606500 (PTB) is annotated by phylogenetic and bioinformatic analysis as the single polypyrimidine tract-binding protein orthologue in Plasmodium falciparum (PMID:30782661). The only experimental evidence linking it to a cellular process is its co-purification with the PfPRMT5-associated protein complex, placing it within the RNA splicing machinery implicated in alternative splicing regulation (PMID:37349497). Beyond this complex membership, no direct functional or mechanistic characterization of PF3D7_0606500 itself — its RNA targets, splicing activity, localization, or phenotype — has been reported in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 2 steps
  1. 2019 Low

    Establishing whether P. falciparum encodes a PTB orthologue was the first step toward asking whether polypyrimidine-tract-based splicing regulation operates in the parasite; bioinformatics identified PF3D7_0606500 as the sole such orthologue.

    Evidence Phylogenetic analysis and bioinformatic annotation, with TGME49_090660 identified as the T. gondii counterpart

    PMID:30782661

    Open questions at the time
    • Computational identification only; no experimental confirmation of PTB activity in Plasmodium
    • No RNA-binding or splicing function demonstrated for the parasite protein
    • No expression, localization, or essentiality data
  2. 2023 Low

    The question of whether PF3D7_0606500 physically associates with splicing machinery was addressed by finding it among proteins co-purifying with PfPRMT5, placing it in a complex regulating alternative splicing.

    Evidence Co-immunoprecipitation / interactome mass spectrometry of cytosolic and nuclear PfPRMT5 pulldowns

    PMID:37349497

    Open questions at the time
    • Single Co-IP/MS experiment identifying PTB as one of many co-purifying proteins, with no reciprocal validation or functional follow-up on PTB itself
    • Direct RNA targets and splicing role of PF3D7_0606500 not defined
    • Whether the association is direct or bridged by other complex members is unknown

Open questions

Synthesis pass · forward-looking unresolved questions
  • The intrinsic molecular function of PF3D7_0606500 — its RNA-binding specificity, splicing substrates, subcellular localization, and requirement for parasite viability — remains uncharacterized.
  • No demonstrated polypyrimidine-tract or RNA binding by the Plasmodium protein
  • No identified splicing targets or regulatory outcomes
  • No knockout, knockdown, or phenotypic data

Mechanism profile

Synthesis pass · controlled-vocabulary classification
Complex memberships
PfPRMT5-associated protein complex / RNA splicing machinery [#0]

Evidence

Reading pass · 2 per-paper findings extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2023 PTB (PF3D7_0606500) was identified as a component of the PfPRMT5-associated protein complex in P. falciparum, co-purifying in immunoprecipitation experiments as a regulator of alternative splicing associated with the RNA splicing machinery. Co-immunoprecipitation / interactome mass spectrometry (cytosolic and nuclear IPs of PfPRMT5) Communications biology Low 37349497
2019 PF3D7_0606500 is annotated as the single PTB orthologue in P. falciparum (with TGME49_090660 as its T. gondii counterpart), identified by phylogenetic/bioinformatic analysis; no functional studies on the Plasmodium PTB orthologue had been published as of this review. Phylogenetic analysis and bioinformatic annotation mBio Low 30782661

Source papers

Stage 0 corpus · 3 papers · ranked by NIH iCite citations
Year Title Journal Citations PMID
2015 A bioinformatic survey of RNA-binding proteins in Plasmodium. BMC genomics 62 26525978
2023 A type II protein arginine methyltransferase regulates merozoite invasion in Plasmodium falciparum. Communications biology 0 37349497
2019 Alternative Splicing in Apicomplexan Parasites. mBio 0 30782661