Evidence map›Paper›PMID 27865713›Full record

ReviewBiochemical pharmacology2017

Platensimycin and platencin: Inspirations for chemistry, biology, enzymology, and medicine.

Jeffrey D Rudolf, Liao-Bin Dong, Ben Shen

Abstract readReview
In one paragraph

Review in Biochemical pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.4field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Uncovering the Cryptic Gene ClusterInternational journal of molecular sciences · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Efficient production of clerodane andBeilstein journal of organic chemistry · 2022
    Article
  17. Bacterial terpenome.Natural product reports · 2021
    Review
  18. Article
  19. Article
  20. Review
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.

Jeffrey D RudolfDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, United States.
Liao-Bin DongDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, United States.
Ben ShenDepartment of Chemistry, The Scripps Research Institute, Jupiter, FL 33458, United States; Department of Molecular Therapeutics, The Scripps Research Institute, Jupiter, FL 33458, United States; Natural Products Library Initiative at The Scripps Research Institute, Jupiter, FL 33458, United States. Electronic address: shenb@scripps.edu.
Scripps Research Institute · US

Funding

Discovery and biosynthesis of diterpenoid natural products in actinomycetalsR01GM114353 · NIGMS · SCRIPPS FLORIDA · PI SHEN, BEN · 2016 to 2019
$1.8M
NIGMS NIH HHS R01 GM114353
6 · The paper itself

Abstract

Natural products have served as the main source of drugs and drug leads, and natural products produced by microorganisms are one of the most prevalent sources of clinical antibiotics. Their unparalleled structural and chemical diversities provide a basis to investigate fundamental biological processes while providing access to a tremendous amount of chemical space. There is a pressing need for novel antibiotics with new mode of actions to combat the growing challenge of multidrug resistant pathogens. This review begins with the pioneering discovery and biological activities of platensimycin (PTM) and platencin (PTN), two antibacterial natural products isolated from Streptomyces platensis. The elucidation of their unique biochemical mode of action, structure-activity relationships, and pharmacokinetics is presented to highlight key aspects of their biological activities. It then presents an overview of how microbial genomics has impacted the field of PTM and PTN and revealed paradigm-shifting discoveries in terpenoid biosynthesis, fatty acid metabolism, and antibiotic and antidiabetic therapies. It concludes with a discussion covering the future perspectives of PTM and PTN in regard to natural products discovery, bacterial diterpenoid biosynthesis, and the pharmaceutical promise of PTM and PTN as antibiotics and for the treatment of metabolic disorders. PTM and PTN have inspired new discoveries in chemistry, biology, enzymology, and medicine and will undoubtedly continue to do so.

Indexed as

AdamantaneAminobenzoatesAminophenolsAnilidesAnimalsAnti-Infective AgentsCommunicable DiseasesHumansPolycyclic CompoundsProtein Structure, SecondaryProtein Structure, TertiaryStructure-Activity RelationshipAdamantaneAminobenzoatesAminophenolsAnilidesAnti-Infective AgentsplatencinplatensimycinPolycyclic CompoundsBiosynthesisFatty acid synthaseMetabolic pathway engineeringPlatencinPlatensimycin

Identifiers

PMID27865713
PMCPMC5410400
OpenAlexW2550070588

What OpenQuestion holds

Textmetadata
LicenceTDM
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.