Evidence map›Paper›PMID 25591746›Full record

ReviewACS chemical biology2015

Defining the orphan functions of lysine acetyltransferases.

David C Montgomery, Alexander W Sorum, Jordan L Meier

Abstract readReview
In one paragraph

Review in ACS chemical biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 44 citations in OpenAlex.

  1. Photoredox-Catalyzed Lysine C(spJournal of the American Chemical Society · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. How Elongator Acetylates tRNA Bases.International journal of molecular sciences · 2020
    Review
  7. Review
  8. Article
  9. Epigenetic regulation by endogenous metabolite pharmacology.Current opinion in chemical biology · 2019
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Global Profiling of Acetyltransferase Feedback Regulation.Journal of the American Chemical Society · 2016
    Article
  18. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

David C MontgomeryNational Cancer Institute , Chemical Biology Laboratory, Frederick, Maryland 21702-1201, United States.
Alexander W Sorum
Jordan L Meier
National Cancer Institute · US

Funding

Targeting Cancer Through Modifications and MetabolismZIABC011488 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MEIER, JORDAN L · 2013 to 2025
$21.3M
6 · The paper itself

Abstract

Long known for their role in histone acetylation, recent studies have demonstrated that lysine acetyltransferases also carry out distinct "orphan" functions. These activities impact a wide range of biological phenomena including metabolism, RNA modification, nuclear morphology, and mitochondrial function. Here, we review the discovery and characterization of orphan lysine acetyltransferase functions. In addition to highlighting the evidence and biological role for these functions in human disease, we discuss the part emerging chemical tools may play in investigating this versatile enzyme superfamily.

Indexed as

Protein Processing, Post-TranslationalAcetylationAcetyl-CoA C-AcetyltransferaseAcetyl Coenzyme AAcetyltransferasesAnimalsHumansLysineN-Terminal Acetyltransferase EN-Terminal Acetyltransferasesp300-CBP-Associated Factorp300-CBP Transcription FactorsRNA Processing, Post-TranscriptionalACAT1 protein, humanAcetyl-CoA C-AcetyltransferaseAcetyl Coenzyme AAcetyltransferasesLysineNAT10 protein, humanN-Terminal Acetyltransferase EN-Terminal Acetyltransferasesp300-CBP-Associated Factorp300-CBP Transcription Factors

Identifiers

PMID25591746
PMCPMC4334240
OpenAlexW2331951716

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.