Evidence map›Paper›PMID 39414231›Full record

ReviewMolecular & cellular proteomics : MCP2024

From Fringe to the Mainstream: How ETD MS Brought O-GlcNAc to the Masses.

Namrata D Udeshi, Gerald W Hart, Chad Slawson

Abstract readReview
In one paragraph

Review in Molecular & cellular proteomics : MCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. HumanResearch square · 2025
    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.

Namrata D UdeshiBroad Institute of MIT and Harvard University, Cambridge, Massachusetts, USA. Electronic address: udeshi@broadinstitute.org.
Gerald W HartDepartment of Biochemistry and Molecular Biology, CCRC, University of Georgia, Athens, Georgia, USA.
Chad SlawsonDepartment Biochemistry, University of Kansas Medical Center, Kansas City, Kansas, USA. Electronic address: cslawson@kumc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

O-GlcNAcylation was identified in the 1980s by Torres and Hart and modifies thousands of cellular proteins, yet the regulatory role of O-GlcNAc is still poorly understood compared to the abundance of mechanistic information known for other cycling post-translational modifications like phosphorylation. Many challenges are associated with studying O-GlcNAcylation and are tied to the technical hurdles with analysis by mass spectrometry. Over the years, many research groups have developed important methods to study O-GlcNAcylation revealing its role in the cell, and this perspective aims to review the challenges and innovations around O-GlcNAc research and chronicle the work by Donald F. Hunt and his laboratory, particularly in development of ETD and its application to this field of research.

Indexed as

AcetylglucosamineMass SpectrometryProtein Processing, Post-TranslationalAnimalsGlycosylationHumansAcetylglucosamineETDglycosylationmass spectrometryO-GlcNAcPTM

Identifiers

PMID39414231
PMCPMC11609545

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.