Before this work the apicomplexan kinetochore was largely undefined; identifying SPC24 as a bona fide component established that these parasites possess a divergent but organized kinetochore, resolving where SPC24 fits within chromosome segregation machinery.
Evidence Interactomics combined with deep homology searches and fluorescence-based subkinetochore localization in Toxoplasma gondii and Plasmodium berghei
- SPC24-specific interactions and localization were not separated from complex-level results
- No direct functional or knockout data establishing SPC24's individual role in spindle attachment or segregation
- No structural model or defined binding partners for SPC24 itself