Evidence map›Paper›PMID 30418763›Full record

ArticleJournal of natural products2018

Puromycins B-E, Naturally Occurring Amino-Nucleosides Produced by the Himalayan Isolate Streptomyces sp. PU-14G.

Muhammad Abbas, Sherif I Elshahawi, Xiachang Wang, Larissa V Ponomareva, Imran Sajid, Khaled A Shaaban, Jon S Thorson

Abstract read
In one paragraph

Article in Journal of natural products, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
  5. Inherently Emissive Puromycin Analogues for Live Cell Labelling.Angewandte Chemie (International ed. in English) · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
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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

7 authors at 3 institutions in 3 countries.

Muhammad AbbasCenter for Pharmaceutical Research and Innovation, College of Pharmacy , University of Kentucky , Lexington , Kentucky 40536 , United States.
Sherif I ElshahawiCenter for Pharmaceutical Research and Innovation, College of Pharmacy , University of Kentucky , Lexington , Kentucky 40536 , United States.ORCID 0000-0003-1879-1552
Xiachang WangCenter for Pharmaceutical Research and Innovation, College of Pharmacy , University of Kentucky , Lexington , Kentucky 40536 , United States.ORCID 0000-0002-1106-1904
Larissa V PonomarevaCenter for Pharmaceutical Research and Innovation, College of Pharmacy , University of Kentucky , Lexington , Kentucky 40536 , United States.
Imran SajidDepartment of Microbiology and Molecular Genetics , University of the Punjab , Quid-i-Azam Campus , Lahore 54590 , Pakistan.
Khaled A ShaabanCenter for Pharmaceutical Research and Innovation, College of Pharmacy , University of Kentucky , Lexington , Kentucky 40536 , United States.
Jon S ThorsonCenter for Pharmaceutical Research and Innovation, College of Pharmacy , University of Kentucky , Lexington , Kentucky 40536 , United States.ORCID 0000-0002-7148-0721
University of Kentucky · USNanjing University of Chinese Medicine · CNUniversity of the Punjab · PK

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Developing Regeneration Resources for a Model AmphibianR24OD021479 · OD · UNIVERSITY OF KENTUCKY · PI THORSON, JON SCOTT, VOSS, STEPHEN RANDAL · 2016 to 2019
$2.3M
NCATS NIH HHS UL1 TR001998NIH HHS R24 OD021479
6 · The paper itself

Abstract

The isolation and structure elucidation of four new naturally occurring amino-nucleoside [puromycins B-E (1-4)] metabolites from a Himalayan isolate ( Streptomyces sp. PU-14-G, isolated from the Bara Gali region of northern Pakistan) is reported. Consistent with prior reports, comparative antimicrobial assays revealed the need for the free 2″-amine for anti-Gram-positive bacteria and antimycobacterial activity. Similarly, comparative cancer cell line cytotoxicity assays highlighted the importance of the puromycin-free 2″-amine and the impact of 3'-nucleoside substitution. These studies extend the repertoire of known naturally occurring puromycins and their corresponding SAR. Notably, 1 represents the first reported naturally occurring bacterial puromycin-related metabolite with a 3'- N-amino acid substitution that differs from the 3'- N-tyrosinyl of classical puromycin-type natural products. This discovery suggests the biosynthesis of 1 in Streptomyces sp. PU-14G may invoke a uniquely permissive amino-nucleoside synthetase and/or multiple synthetases and sets the stage for further studies to elucidate, and potentially exploit, new biocatalysts for puromycin chemoenzymatic diversification.

Indexed as

Gram-Positive BacteriaMicrobial Sensitivity TestsMolecular StructureMycobacteriumNucleosidesPakistanPuromycinStreptomycesNucleosidesPuromycin

Identifiers

PMID30418763
PMCPMC6393767
OpenAlexW2900620514

What OpenQuestion holds

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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.