Component

Monoacetylated histone H3/H4 assay peptides

Experimental histone peptides bearing a single acetylated lysine; not free dietary lysine.

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. Human SIRT2 deacetylated monoacetylated histone peptides in the NAD-consuming reaction producing nicotinamide and O-acetyl-ADP-ribose.

    Experimental context and source evidence
    cross_nutrient
    false
    evidence_span
    {"source_cache": "artifacts/niacin-consumption-sources/sirt22004.abstract.txt", "locator": "Indexed abstract", "start_char": 0, "end_char": 1423, "file_sha256": "a84f7d25c6e518d3317d4b0a41df8d8ac447cd3ef2966815c9818ca63116ef7f", "text_sha256": "a84f7d25c6e518d3317d4b0a41df8d8ac447cd3ef2966815c9818ca63116ef7f"}
    experimental_model
    Recombinant enzyme and monoacetylated histone H3/H4 peptide assays
    exposure
    Human SIRT2; yeast Sir2/Hst2 were also studied separately
    limitations
    Indexed abstract; rapid-kinetic details are not assigned to human SIRT2 individually. No dietary or longevity inference.
    nutrient_topic
    Niacin research collection; topical membership is not evidence of a direct dietary effect. · Niacin (vitamin B3)
    organism
    Human
    plain_language
    SIRT2 consumes NAD while removing acetyl groups from histone peptides.
    primary_references
    [b3-cons-sirt22004] Substrate specificity and kinetic mechanism of the Sir2 family of NAD+-dependent histone/protein deacetylases. (2004). https://pubmed.ncbi.nlm.nih.gov/15274642/ DOI: 10.1021/bi049592e
    tissue_or_cell_type
    Cell-free assay

    Niacin: NAD metabolism, deficiency and nutrient interactions (2026-09-17) · lines 551–563

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Recombinant enzyme and monoacetylated histone H3/H4 peptide assays · source_derived_draft · unverified_draft

    ### b3-cons-sirt2-reaction Human SIRT2 deacetylated monoacetylated histone peptides in the NAD-consuming reaction producing nicotinamide and O-acetyl-ADP-ribose. Condition category: normal nutrient_topic: Niacin research collection; topical membership is not evidence of a direct dietary effect. plain_language: SIRT2 consumes NAD while removing acetyl groups from histone peptides. organism: Human tissue_or_cell_type: Cell-free assay experimental_model: Recombinant enzyme and monoacetylated histone H3/H4 peptide assays limitations: Indexed abstract; rapid-kinetic details are not assigned to human SIRT2 individually. No dietary or longevity inference. exposure: Human SIRT2; yeast Sir2/Hst2 were also studied separately cross_nutrient: false evidence_span: {"source_cache": "artifacts/niacin-consumption-sources/sirt22004.abstract.txt", "locator": "Indexed abstract", "start_char": 0, "end_char": 1423, "file_sha256": "a84f7d25c6e518d3317d4b0a41df8d8ac447cd3ef2966815c9818ca63116ef7f", "text_sha256": "a84f7d25c6e518d3317d4b0a41df8d8ac447cd3ef2966815c9818ca63116ef7f"} [b3-cons-sirt22004] Substrate specificity and kinetic mechanism of the Sir2 family of NAD+-dependent histone/protein deacetylases. (2004). https://pubmed.ncbi.nlm.nih.gov/15274642/ DOI: 10.1021/bi049592e
    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