Component

Human proton-coupled folate transporter / SLC46A1

Human proton-coupled folate transporter / SLC46A1; species and subcellular isoforms retained separately.

2 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. Expression of human PCFT produced high-affinity, proton-coupled folate uptake with enhanced activity at acidic pH.

    Experimental context and source evidence
    experimental_model
    Human transporter expression, electrophysiology and affected family
    exposure
    Folate substrates across pH conditions
    limitations
    Expression-system kinetics are not whole-intestine absorption fractions.
    nutrient_topic
    Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. · Folate (vitamin B9)
    organism
    Human transporter in cellular/oocyte expression systems
    plain_language
    PCFT uses acidic conditions to help folate enter cells.
    primary_references
    [qiu2006] Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption (2006). https://pubmed.ncbi.nlm.nih.gov/17129779/ DOI: 10.1016/j.cell.2006.09.041
    tissue_or_cell_type
    Membrane transport models
    transport_effect
    raises Recorded as high-affinity proton-coupled folate uptake.
    transport_pool
    the expressing cell Recorded as high-affinity proton-coupled folate uptake.

    Folate and folic acid: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 131–141

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human transporter expression, electrophysiology and affected family · source_derived_draft · unverified_draft

    ### folate-pcft-proton-coupled-entry Expression of human PCFT produced high-affinity, proton-coupled folate uptake with enhanced activity at acidic pH. Condition category: normal nutrient_topic: Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. plain_language: PCFT uses acidic conditions to help folate enter cells. organism: Human transporter in cellular/oocyte expression systems tissue_or_cell_type: Membrane transport models experimental_model: Human transporter expression, electrophysiology and affected family limitations: Expression-system kinetics are not whole-intestine absorption fractions. exposure: Folate substrates across pH conditions [qiu2006] Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption (2006). https://pubmed.ncbi.nlm.nih.gov/17129779/ DOI: 10.1016/j.cell.2006.09.041
    Complete structured claim and evidence

Where it participates (unsigned role)

  1. A PCFT loss-of-function mutation in the studied family established a genetic cause of hereditary folate malabsorption.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    experimental_model
    Human transporter expression, electrophysiology and affected family
    exposure
    Inherited mutation
    limitations
    Rare familial disorder; not dietary withdrawal.
    nutrient_topic
    Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. · Folate (vitamin B9)
    organism
    Homo sapiens
    plain_language
    An inherited transport defect can reduce folate absorption.
    primary_references
    [qiu2006] Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption (2006). https://pubmed.ncbi.nlm.nih.gov/17129779/ DOI: 10.1016/j.cell.2006.09.041
    tissue_or_cell_type
    Intestinal absorption and family genetics
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Folate and folic acid: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 143–153

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human transporter expression, electrophysiology and affected family · source_derived_draft · unverified_draft

    ### folate-pcft-inherited-malabsorption A PCFT loss-of-function mutation in the studied family established a genetic cause of hereditary folate malabsorption. Condition category: machinery_impairment nutrient_topic: Folate and folic acid research collection; topical membership is not evidence of a direct dietary effect. plain_language: An inherited transport defect can reduce folate absorption. organism: Homo sapiens tissue_or_cell_type: Intestinal absorption and family genetics experimental_model: Human transporter expression, electrophysiology and affected family limitations: Rare familial disorder; not dietary withdrawal. exposure: Inherited mutation [qiu2006] Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption (2006). https://pubmed.ncbi.nlm.nih.gov/17129779/ DOI: 10.1016/j.cell.2006.09.041
    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