Evidence map›Paper›PMID 32175720›Full record

ArticleACS chemical biology2020

Biosynthetic Incorporation of Site-Specific Isotopes in β-Lactam Antibiotics Enables Biophysical Studies.

Jacek Kozuch, Samuel H Schneider, Steven G Boxer

Open access · greenAbstract read
In one paragraph

Article in ACS chemical biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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.

Jacek KozuchDepartment of Chemistry, Stanford University, Stanford, California 94305-5012, United States.
Samuel H SchneiderDepartment of Chemistry, Stanford University, Stanford, California 94305-5012, United States.ORCID 0000-0002-5792-4015
Steven G BoxerDepartment of Chemistry, Stanford University, Stanford, California 94305-5012, United States.ORCID 0000-0001-9167-4286
Stanford University · US

Funding

Biophysical Studies of Macromolecules and Molecular AssembliesR35GM118044 · NIGMS · STANFORD UNIVERSITY · PI STEVEN G. BOXER · 2016 to 2026
$7.2M
NIGMS NIH HHS R35 GM118044
6 · The paper itself

Abstract

A biophysical understanding of the mechanistic, chemical, and physical origins underlying antibiotic action and resistance is vital to the discovery of novel therapeutics and the development of strategies to combat the growing emergence of antibiotic resistance. The site-specific introduction of stable-isotope labels into chemically complex natural products is particularly important for techniques such as NMR, IR, mass spectrometry, imaging, and kinetic isotope effects. Toward this goal, we developed a biosynthetic strategy for the site-specific incorporation of

Indexed as

Anti-Bacterial Agentsbeta-Lactamasesbeta-LactamsBinding SitesCarbon IsotopesCefotaximeCephalosporinsDrug DiscoveryDrug Resistance, MicrobialPenicillin GPenicilliumProtein ConformationAnti-Bacterial Agentsbeta-Lactamasesbeta-lactamase TEM-1beta-LactamsCarbon IsotopesCefotaximecephalosporin CCephalosporinsPenicillin G

Identifiers

PMID32175720
PMCPMC7229998
OpenAlexW3011358199

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.