Component

Human CK2 alpha/beta reconstituted holoenzyme

Human CK2 alpha/beta reconstituted holoenzyme

1 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What acts on it

  1. Apigenin inhibited this human CK2 preparation with IC50 1.5 micromolar using P2B substrate and 0.8 micromolar using the peptide substrate.

    Experimental context and source evidence
    evidence_access
    Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    experimental_contrast
    {"intervention": "Apigenin concentration series", "comparator": "No inhibitor", "endpoint": "Apigenin inhibited this human CK2 preparation with IC50 1.5 micromolar using P2B substrate and 0.8 micromolar using the peptide substrate.", "effect_direction": "decrease", "combination": "single", "conditions": []} Explicit extracted experimental comparison; recorded from source.
    experimental_model
    Recombinant human CK2; ATP 20 micromolar; Table 1.
    interpretation_status
    Recorded from source with stated access limits; ungraded, not independent replication.
    limitations
    Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation.
    nutrient_topic
    Apigenin collection; exact intervention and molecular form govern interpretation. · Apigenin
    plain_language
    Apigenin inhibited this human CK2 preparation with IC50 1.5 micromolar using P2B substrate and 0.8 micromolar using the peptide substrate.
    primary_references
    Inhibitory influence of natural flavonoids on human protein kinase CK2 isoforms: effect of the regulatory subunit. | https://pubmed.ncbi.nlm.nih.gov/29188536/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC6002439/ | https://doi.org/10.1007/s11010-017-3228-1
    source_locator
    Reviewed reference api-ck2-alpha-holo; Subunit identity and assay substrate are part of the potency result; no universal IC50 or physiological ATP correction is implied.

    Apigenin: detailed mechanisms of action (reviewed 10 October 2026) · lines 616–622

    AI-assisted original curation of primary studies; claim-local access and experimental limitations stated. Includes original-draft correction history. No independent replication claimed. · supports · Recombinant human CK2; ATP 20 micromolar; Table 1. · Recorded from source · Recorded from source

    ### api-ck2-alpha-holo Apigenin inhibited this human CK2 preparation with IC50 1.5 micromolar using P2B substrate and 0.8 micromolar using the peptide substrate. Subunit identity and assay substrate are part of the potency result; no universal IC50 or physiological ATP correction is implied. Model and exposure: Recombinant human CK2; ATP 20 micromolar; Table 1. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Inhibitory influence of natural flavonoids on human protein kinase CK2 isoforms: effect of the regulatory subunit. | 2018 | https://pubmed.ncbi.nlm.nih.gov/29188536/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC6002439/ | https://doi.org/10.1007/s11010-017-3228-1 | Access: Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.