Evidence map›Paper›PMID 37615926›Full record

ReviewChembiochem : a European journal of chemical biology2023

Current State-of-the-Art Toward Chemoenzymatic Synthesis of Polyketide Natural Products.

Thaddeus Q Paulsel, Gavin J Williams

Abstract readReview
In one paragraph

Review in Chembiochem : a European journal of chemical biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  3. Engineering an Acyl-CoA Ligase With Enhanced Activity Toward Synthetic CoA Alternatives.Chembiochem : a European journal of chemical biology · 2026
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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

2 authors.

Thaddeus Q PaulselDepartment of Chemistry, NC State University Dabney Hall, Room 208, Campus Box 8204, 2620 Yarbrough Dr., NC State University, Raleigh, NC 27695, USA.ORCID 0000-0002-2010-120X
Gavin J WilliamsDepartment of Chemistry, NC State University Dabney Hall, Room 208, Campus Box 8204, 2620 Yarbrough Dr., NC State University, Raleigh, NC 27695, USA.ORCID 0000-0003-2172-9063

Funding

Designer biosensors for directed evolution of macrolide biosynthetic enzymesR01GM124112 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI CROPP, THOMAS ASHTON, WILLIAMS, GAVIN J · 2018 to 2021
$1.1M
NIGMS NIH HHS R01 GM124112NIH HHS GM124112
6 · The paper itself

Abstract

Polyketide natural products have significant promise as pharmaceutical targets for human health and as molecular tools to probe disease and complex biological systems. While the biosynthetic logic of polyketide synthases (PKS) is well-understood, biosynthesis of designer polyketides remains challenging due to several bottlenecks, including substrate specificity constraints, disrupted protein-protein interactions, and protein solubility and folding issues. Focusing on substrate specificity, PKSs are typically interrogated using synthetic thioesters. PKS assembly lines and their products offer a wealth of information when studied in a chemoenzymatic fashion. This review provides an overview of the past two decades of polyketide chemoenzymatic synthesis and their contributions to the field of chemical biology. These synthetic strategies have successfully yielded natural product derivatives while providing critical insights into enzymatic promiscuity and mechanistic activity.

Indexed as

Biological ProductsPolyketidesHumansPolyketide SynthasesSecondary MetabolismSubstrate SpecificityBiological ProductsPolyketidesPolyketide Synthasesbioorganic chemistrybiosynthesisenzymespolyketidessynthetic biology

Identifiers

PMID37615926
PMCPMC10964317

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Registered trials

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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.