Evidence map›Paper›PMID 25402849›Full record

ReviewACS chemical biology2015

Protein prenylation: enzymes, therapeutics, and biotechnology applications.

Charuta C Palsuledesai, Mark D Distefano

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 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

138 citing papers in PubMed, 256 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Host prenylation promotes membrane association of theMicrobiology (Reading, England) · 2026
    Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. De Novo Discovery of Prenylated Macrocyclic Peptide Ligands.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. ACS chemical biology · 2025
    Article
  19. Article
  20. Review

78 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Charuta C PalsuledesaiDepartment of Chemistry, University of Minnesota , Minneapolis, Minnesota 55455, United States.
Mark D Distefano
University of Minnesota · US

Funding

Enzymatic Protein LabelingR01GM084152 · NIGMS · UNIVERSITY OF MINNESOTA · PI DISTEFANO, MARK D · 2010 to 2019
$2.6M
LIGHT ACTIVATED ANTI-CANCER DRUGSR21CA185783 · NCI · UNIVERSITY OF MINNESOTA · PI DISTEFANO, MARK D · 2014 to 2015
$338k
NCI NIH HHS CA185783NCI NIH HHS R21 CA185783NIGMS NIH HHS GM084152NIGMS NIH HHS R01 GM084152
6 · The paper itself

Abstract

Protein prenylation is a ubiquitous covalent post-translational modification found in all eukaryotic cells, comprising attachment of either a farnesyl or a geranylgeranyl isoprenoid. It is essential for the proper cellular activity of numerous proteins, including Ras family GTPases and heterotrimeric G-proteins. Inhibition of prenylation has been extensively investigated to suppress the activity of oncogenic Ras proteins to achieve antitumor activity. Here, we review the biochemistry of the prenyltransferase enzymes and numerous isoprenoid analogs synthesized to investigate various aspects of prenylation and prenyltransferases. We also give an account of the current status of prenyltransferase inhibitors as potential therapeutics against several diseases including cancers, progeria, aging, parasitic diseases, and bacterial and viral infections. Finally, we discuss recent progress in utilizing protein prenylation for site-specific protein labeling for various biotechnology applications.

Indexed as

AnimalsBiotechnologyDimethylallyltranstransferaseEnzyme InhibitorsHumansProtein Prenylationras ProteinsSubstrate SpecificityTerpenesDimethylallyltranstransferaseEnzyme Inhibitorsras ProteinsTerpenes

Identifiers

PMID25402849
PMCPMC4301080
OpenAlexW2324956847

What Socratic 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 Socratic graph.