Component

Human glycine decarboxylase / GLDC

Human glycine decarboxylase / GLDC

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. Human GLDC cDNA sequencing identified a conserved PLP-binding lysine region corresponding to the chicken enzyme.

    Human glycine decarboxylase / GLDC → PLP source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Human and chicken cDNA cloning and sequence comparison
    limitations
    Sequence evidence; human catalytic rates were not established by this cloning study.
    nutrient_topic
    Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B6
    organism
    Homo sapiens
    plain_language
    The human enzyme retains the conserved B6-binding machinery.
    primary_references
    [b6-gldc-1991] The glycine cleavage system. Molecular cloning of the chicken and human glycine decarboxylase cDNAs and some characteristics involved in the deduced protein structures. (1991). https://pubmed.ncbi.nlm.nih.gov/1993704/ DOI: 10.1016/s0021-9258(18)49991-7
    tissue_or_cell_type
    Cloned human GLDC cDNA and deduced protein sequence

    Vitamin B6: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 671–680

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human and chicken cDNA cloning and sequence comparison · source_derived_draft · unverified_draft

    ### b6-met-human-gldc-plp-site Human GLDC cDNA sequencing identified a conserved PLP-binding lysine region corresponding to the chicken enzyme. Condition category: normal nutrient_topic: Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. plain_language: The human enzyme retains the conserved B6-binding machinery. organism: Homo sapiens tissue_or_cell_type: Cloned human GLDC cDNA and deduced protein sequence experimental_model: Human and chicken cDNA cloning and sequence comparison limitations: Sequence evidence; human catalytic rates were not established by this cloning study. [b6-gldc-1991] The glycine cleavage system. Molecular cloning of the chicken and human glycine decarboxylase cDNAs and some characteristics involved in the deduced protein structures. (1991). https://pubmed.ncbi.nlm.nih.gov/1993704/ DOI: 10.1016/s0021-9258(18)49991-7
    Complete structured claim and evidence

Where it participates (unsigned role)

  1. Human AMT transfers the aminomethyl-lipoyl intermediate's carbon to tetrahydrofolate, yielding 5,10-methylene-THF, ammonia and reduced H-protein.

    Experimental context and source evidence
    cross_nutrient
    B6-dependent GLDC precedes lipoyl-carrier transfer and folate-dependent AMT chemistry.
    experimental_model
    Purified human AMT structures and mutational analyses
    limitations
    AMT is the directly examined human enzyme; this study did not test dietary B6 depletion or the entire pathway flux.
    nutrient_topic
    Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B6
    organism
    Homo sapiens
    plain_language
    Glycine cleavage connects its B6-dependent first step to a separate folate-dependent step.
    primary_references
    [b6-amt-2005] Crystal structure of human T-protein of glycine cleavage system at 2.0 A resolution and its implication for understanding non-ketotic hyperglycinemia. (2005). https://pubmed.ncbi.nlm.nih.gov/16051266/ DOI: 10.1016/j.jmb.2005.06.056
    tissue_or_cell_type
    Purified recombinant protein; no intact tissue

    Vitamin B6: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 682–692

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Purified human AMT structures and mutational analyses · source_derived_draft · unverified_draft

    ### b6-met-amt-onecarbon Human AMT transfers the aminomethyl-lipoyl intermediate's carbon to tetrahydrofolate, yielding 5,10-methylene-THF, ammonia and reduced H-protein. Condition category: normal nutrient_topic: Vitamin B6 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Glycine cleavage connects its B6-dependent first step to a separate folate-dependent step. organism: Homo sapiens tissue_or_cell_type: Purified recombinant protein; no intact tissue experimental_model: Purified human AMT structures and mutational analyses limitations: AMT is the directly examined human enzyme; this study did not test dietary B6 depletion or the entire pathway flux. cross_nutrient: B6-dependent GLDC precedes lipoyl-carrier transfer and folate-dependent AMT chemistry. [b6-amt-2005] Crystal structure of human T-protein of glycine cleavage system at 2.0 A resolution and its implication for understanding non-ketotic hyperglycinemia. (2005). https://pubmed.ncbi.nlm.nih.gov/16051266/ DOI: 10.1016/j.jmb.2005.06.056
    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