Evidence map›Paper›PMID 33780244›Full record

ArticleJournal of the American Chemical Society2021

Dirigent Proteins Guide Asymmetric Heterocoupling for the Synthesis of Complex Natural Product Analogues.

Stacie S Kim, Elizabeth S Sattely

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  10. Uniform binding and negative catalysis at the origin of enzymes.Protein science : a publication of the Protein Society · 2022
    Article
  11. Review
  12. The Transformative Power of Biocatalysis in Convergent Synthesis.Journal of the American Chemical Society · 2022
    Review
  13. Review
  14. 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

2 authors at 2 institutions in 1 country.

Stacie S KimDepartment of Chemical Engineering, Stanford University, Stanford, California 94305, United States.ORCID 0000-0003-4755-0598
Elizabeth S SattelyDepartment of Chemical Engineering and Howard Hughes Medical Institute, Stanford University, Stanford, California 94305, United States.ORCID 0000-0002-7352-859X
Howard Hughes Medical Institute · USStanford University · US

Funding

Synthetic biology tools for scalable production of medicinal plant terpenesR01AT010593 · NCCIH · STANFORD UNIVERSITY · PI KEASLING, JAY D, LANGE, BERND MARKUS · 2019 to 2023
$3.5M
Discovery and Engineering of Plant Natural Product PathwaysR01GM121527 · NIGMS · STANFORD UNIVERSITY · PI SATTELY, ELIZABETH SUSAN · 2017 to 2025
$2.3M
Howard Hughes Medical InstituteNCCIH NIH HHS R01 AT010593NIGMS NIH HHS R01 GM121527
6 · The paper itself

Abstract

Phenylpropanoids are a class of abundant building blocks found in plants and derived from phenylalanine and tyrosine. Phenylpropanoid polymerization leads to the second most abundant biopolymer lignin while stereo- and site-selective coupling generates an array of lignan natural products with potent biological activity, including the topoisomerase inhibitor and chemotherapeutic etoposide. A key step in etoposide biosynthesis involves a plant dirigent protein that promotes selective dimerization of coniferyl alcohol, a common phenylpropanoid, to form (+)-pinoresinol, a critical C

Indexed as

Biological ProductsLignansOxidation-ReductionPhenolsPlant ProteinsPodophyllumProteinsStereoisomerismBiological Productsconiferyl alcoholLignansPhenolsPlant ProteinsProteins

Identifiers

PMID33780244
PMCPMC8450019
OpenAlexW3140445838

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.