Affinage · Plasmodium

PF3D7_0103000

vacuolar protein sorting-associated protein VTA1, putative

Audit flag: identity unverified
Annotated
2026-09-07
1 papers in source corpus 1 papers cited in narrative 1 extracted findings

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

PF3D7_0103000 (VTA1/PfVta1) functions as a cofactor of the ESCRT machinery in Plasmodium falciparum, where it directly stimulates the enzymatic activity of PfVPS4, the core AAA-ATPase of the ESCRT complex, as demonstrated by in vitro biochemical reconstitution (PMID:41957628). Beyond this cofactor role in enhancing PfVPS4 ATPase activity (PMID:41957628), no further mechanistic detail — including its own domain architecture, oligomeric state, localization, or cellular phenotype — has been characterized for PF3D7_0103000 in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2026 Medium

    It was unknown whether P. falciparum possessed a functional VPS4 cofactor; reconstituting PfVta1 with PfVPS4 in vitro established that PF3D7_0103000 acts as a genuine ATPase-stimulating cofactor of the parasite ESCRT AAA-ATPase.

    Evidence In vitro protein purification and enzyme kinetics assays measuring PfVPS4 ATPase activity with and without the PfVta1 cofactor

    PMID:41957628

    Open questions at the time
    • Single lab, single in vitro study without independent replication
    • No cellular or genetic evidence that this cofactor activity operates in vivo in the parasite
    • Interaction interface, binding stoichiometry, and localization of PfVta1 are undefined

Open questions

Synthesis pass · forward-looking unresolved questions
  • Whether PfVta1 is essential for parasite ESCRT function, membrane remodeling, or viability, and how it engages PfVPS4 structurally, remains unaddressed in the available corpus.
  • No genetic knockout or knockdown phenotype reported
  • No structural model of the PfVta1–PfVPS4 complex
  • No subcellular localization data for PfVta1

Mechanism profile

Synthesis pass · controlled-vocabulary classification
Partners
Complex memberships
ESCRT machinery (as PfVPS4 cofactor)

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2026 PF3D7_0103000 (VTA1/PfVta1) acts as a cofactor that significantly enhances the ATPase activity of PfVPS4, the core AAA-ATPase of the ESCRT complex in P. falciparum, as demonstrated by in vitro biochemical assays. In vitro protein purification and enzyme kinetics assays measuring PfVPS4 ATPase activity in the presence of PfVta1 cofactor Parasites & vectors Medium 41957628

Source papers

Stage 0 corpus · 1 paper · ranked by NIH iCite citations
Year Title Journal Citations PMID
2026 PfVPS4, an ESCRT AAA-ATPase, is essential for asexual proliferation and gametocyte sexual conversion in Plasmodium falciparum. Parasites & vectors 0 41957628