Component

Human ZnT5-ZnT6 heterodimer

Human SLC30A5/SLC30A6 heterodimer used to restore TNAP activation in engineered chicken cells.

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 it acts on

  1. The ZnT5-ZnT6 and ZnT7 complexes support TNAP conversion from apoenzyme to zinc-loaded active enzyme in the early secretory pathway.

    Experimental context and source evidence
    cross_nutrient
    false
    experimental_model
    Engineered chicken DT40 cells with ZnT gene disruption and transporter re-expression; TNAP activation
    exposure
    ZnT gene disruption and transporter re-expression comparisons.
    limitations
    Primary abstract-level evidence in engineered chicken DT40 cells with transporter complementation. Not a human dietary deficiency or supplementation trial; assay exposure amounts and mutant-specific residue effects are not inferred.
    nutrient_topic
    Zinc research collection; topical membership is not evidence of a direct dietary effect. · Zinc
    organism
    Gallus gallus cell model with human proteins
    plain_language
    Specific transporter complexes deliver zinc while TNAP matures.
    primary_references
    [zinc-enz-znt-tnap2011] Tissue nonspecific alkaline phosphatase is activated via a two-step mechanism by zinc transport complexes in the early secretory pathway. (2011). https://pubmed.ncbi.nlm.nih.gov/21402707/ DOI: 10.1074/jbc.m111.227173
    tissue_or_cell_type
    Chicken DT40 early secretory pathway; human transporter complementation

    Zinc: transport, enzyme loading, deficiency and nutrient interactions (2026-09-17) · lines 768–779

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Engineered chicken DT40 cells with ZnT gene disruption and transporter re-expression; TNAP activation · source_derived_draft · unverified_draft

    ### zinc-enz-znt-specific-maturation The ZnT5-ZnT6 and ZnT7 complexes support TNAP conversion from apoenzyme to zinc-loaded active enzyme in the early secretory pathway. Condition category: normal nutrient_topic: Zinc research collection; topical membership is not evidence of a direct dietary effect. plain_language: Specific transporter complexes deliver zinc while TNAP matures. organism: Gallus gallus cell model with human proteins tissue_or_cell_type: Chicken DT40 early secretory pathway; human transporter complementation experimental_model: Engineered chicken DT40 cells with ZnT gene disruption and transporter re-expression; TNAP activation limitations: Primary abstract-level evidence in engineered chicken DT40 cells with transporter complementation. Not a human dietary deficiency or supplementation trial; assay exposure amounts and mutant-specific residue effects are not inferred. exposure: ZnT gene disruption and transporter re-expression comparisons. cross_nutrient: false [zinc-enz-znt-tnap2011] Tissue nonspecific alkaline phosphatase is activated via a two-step mechanism by zinc transport complexes in the early secretory pathway. (2011). https://pubmed.ncbi.nlm.nih.gov/21402707/ DOI: 10.1074/jbc.m111.227173
    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.

    Evidence, AI assistance and curation standards