Affinage · Toxoplasma gondii

CDC20

cell division cycle protein CDC20, putative · UniProt A0A125YU43

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

Mechanistic narrative

Synthesis pass · prose summary of the discoveries below

In Toxoplasma gondii, TgCdc20 was identified as a candidate phosphorylation substrate of the TgCrk4-TgCyc4 CDK complex in a global phosphoproteome screen, placing it downstream of cell cycle kinase signaling (PMID:38600241). Beyond this single phosphoproteomic association, no direct mechanistic detail of TgCdc20's own function, partners, or role has been characterized in the available corpus.

Mechanistic history

Synthesis pass · year-by-year structured walk · 1 step
  1. 2024 Low

    To map the substrate landscape of the cell cycle kinase TgCrk4, a phosphoproteome screen tested which proteins are phosphorylated in a TgCrk4-dependent manner, and identified TgCdc20 as a candidate substrate — the first mechanistic link placing TgCdc20 under CDK-complex regulation.

    Evidence Global mass spectrometry-based phosphoproteome analysis of TgCrk4-TgCyc4 substrates in Toxoplasma gondii

    PMID:38600241

    Open questions at the time
    • Single phosphoproteomics screen without in vitro kinase assay or phosphosite mutagenesis to validate TgCdc20 as a bona fide direct substrate
    • No functional characterization of TgCdc20's own activity, interactors, or cell cycle role
    • Whether phosphorylation regulates TgCdc20 activity or localization is untested

Open questions

Synthesis pass · forward-looking unresolved questions
  • The molecular function of TgCdc20, its downstream effectors, and the functional consequence of its phosphorylation by TgCrk4-TgCyc4 remain unestablished.
  • No experimental determination of TgCdc20's own biochemical activity
  • No identified binding partners or substrates of TgCdc20
  • No genetic or phenotypic evidence for its role in cell cycle progression

Mechanism profile

Synthesis pass · controlled-vocabulary classification

Evidence

Reading pass · 1 per-paper finding extracted from the source corpus
Year Finding Method Journal Conf PMIDs
2024 TgCdc20 was identified as a phosphorylation substrate of the TgCrk4-TgCyc4 CDK complex, as determined by global phosphoproteome analysis of TgCrk4 substrates in Toxoplasma gondii. Global phosphoproteome analysis (mass spectrometry-based substrate identification) The EMBO journal Low 38600241

Source papers

Stage 0 corpus · 1 paper · ranked by NIH iCite citations
Year Title Journal Citations PMID
2024 The Crk4-Cyc4 complex regulates G2/M transition in Toxoplasma gondii. The EMBO journal 16 38600241