Evidence map›Paper›PMID 30605564›Full record

ReviewChembiochem : a European journal of chemical biology2019

Natural Voltage-Gated Sodium Channel Ligands: Biosynthesis and Biology.

April L Lukowski, Alison R H Narayan

Abstract readReview
In one paragraph

Review in Chembiochem : a European journal of chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. 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.

April L LukowskiProgram in Chemical Biology, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI, 48109, USA.
Alison R H NarayanLife Sciences Institute, University of Michigan, 210 Washtenaw Ave., Ann Arbor, MI, 48109, USA.ORCID 0000-0001-8290-0077

Funding

Undergrad Supplement: Expanding the synthetic utility of natural product biosynthetic enzymesR35GM124880 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alison Narayan · 2017 to 2026
$4.5M
Biocatalytic approaches to antiepileptic drug targetsF31NS111906 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUKOWSKI, APRIL · 2019 to 2020
$49k
NIGMS NIH HHS R35 GM124880NINDS NIH HHS F31 NS111906
6 · The paper itself

Abstract

Natural product biosynthetic pathways are composed of enzymes that use powerful chemistry to assemble complex molecules. Small molecule neurotoxins are examples of natural products with intricate scaffolds which often have high affinities for their biological targets. The focus of this Minireview is small molecule neurotoxins targeting voltage-gated sodium channels (VGSCs) and the state of knowledge on their associated biosynthetic pathways. There are three small molecule neurotoxin receptor sites on VGSCs associated with three different classes of molecules: guanidinium toxins, alkaloid toxins, and ladder polyethers. Each of these types of toxins have unique structural features which are assembled by biosynthetic enzymes and the extent of information known about these enzymes varies among each class. The biosynthetic enzymes involved in the formation of these toxins have the potential to become useful tools in the efficient synthesis of VGSC probes.

Indexed as

AnimalsLigandsMolecular StructureNeurotoxinsPlantsSodium Channel BlockersVoltage-Gated Sodium ChannelsLigandsNeurotoxinsSodium Channel BlockersVoltage-Gated Sodium Channelsbiocatalysisbiosynthesisenzymesneurotoxinsvoltage-gated sodium channels

Identifiers

PMID30605564
PMCPMC6579537

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.