Component

Human MMADHC segment after Met116

N-terminally shortened MMADHC sequence examined using translation-reinitiation/expression constructs.

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. MMADHC expression/translation-reinitiation experiments in cblD patient fibroblasts indicated that sequence after Met116 was sufficient to support methylcobalamin synthesis.

    Human MMADHC segment after Met116 → Methylcobalamin source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    cross_nutrient
    false
    evidence_location
    Abstract
    experimental_model
    Human cblD fibroblast construct-rescue study
    exposure
    MMADHC constructs changing stop codons or downstream translation starts
    limitations
    Abstract-level domain inference; no claim of an independently purified physiological isoform.
    nutrient_topic
    Vitamin B12 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B12 (cobalamins)
    organism
    Homo sapiens
    plain_language
    The later portion of MMADHC could support the methyl-B12 branch in these cells.
    primary_references
    [stucki-2012-mmad-routing] Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism (2012). https://pubmed.ncbi.nlm.nih.gov/22156578/ DOI: 10.1093/hmg/ddr579
    tissue_or_cell_type
    Patient fibroblasts
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Vitamin B12: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 851–863

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human cblD fibroblast construct-rescue study · source_derived_draft · unverified_draft

    ### b12-mmad-after116-methyl MMADHC expression/translation-reinitiation experiments in cblD patient fibroblasts indicated that sequence after Met116 was sufficient to support methylcobalamin synthesis. Condition category: machinery_impairment nutrient_topic: Vitamin B12 research collection; topical membership is not evidence of a direct dietary effect. plain_language: The later portion of MMADHC could support the methyl-B12 branch in these cells. organism: Homo sapiens tissue_or_cell_type: Patient fibroblasts experimental_model: Human cblD fibroblast construct-rescue study limitations: Abstract-level domain inference; no claim of an independently purified physiological isoform. exposure: MMADHC constructs changing stop codons or downstream translation starts cross_nutrient: false evidence_location: Abstract [stucki-2012-mmad-routing] Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism (2012). https://pubmed.ncbi.nlm.nih.gov/22156578/ DOI: 10.1093/hmg/ddr579
    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