Evidence map›Paper›PMID 26062397›Full record

ReviewFuture medicinal chemistry2015

SecA: a potential antimicrobial target.

Arpana S Chaudhary, Weixuan Chen, Jinshan Jin, Phang C Tai, Binghe Wang

Open access · greenAbstract readReview
In one paragraph

Review in Future medicinal chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 32% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Screening of Novel Inhibitors Targeting the Non-ATP-binding Domain ofMedicinal chemistry (Shariqah (United Arab Emirates)) · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. RSC advances · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Methods of IdentifyingPathogens (Basel, Switzerland) · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Mutational Evolution ofFrontiers in genetics · 2018
    Article
  16. Article
  17. Article
  18. 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

5 authors at 1 institution in 1 country.

Arpana S ChaudharyDepartment of Chemistry, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.
Weixuan ChenDepartment of Chemistry, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.
Jinshan JinDepartment of Biology, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.
Phang C TaiDepartment of Biology, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.
Binghe WangDepartment of Chemistry, Center for Diagnostics & Therapeutics, & Center for Biotechnology & Drug Design, Georgia State University, Atlanta, GA 30303, USA.
Georgia State University · US

Funding

Examining SecA as a Potential Target for Treating Gram-positive BacteriaR56AI104168 · NIAID · GEORGIA STATE UNIVERSITY · PI EICHENBAUM, ZEHAVA, TAI, PHANG C. · 2014 to 2014
$444k
NIAID NIH HHS AI104168NIAID NIH HHS R56 AI104168
6 · The paper itself

Abstract

There is a consensus in the medical profession of the pressing need for novel antimicrobial agents due to issues related to drug resistance. In practice, solutions to this problem to a large degree lie with the identification of new and vital targets in bacteria and subsequently designing their inhibitors. We consider SecA a very promising antimicrobial target. In this review, we compile and analyze information available on SecA to show that inhibition of SecA has a multitude of consequences. Furthermore, we discuss issues critical to the design and evaluation of SecA inhibitors.

Indexed as

Adenosine TriphosphatasesAnti-Bacterial AgentsBacterial ProteinsDrug DesignEnzyme InhibitorsHumansMembrane Transport ProteinsModels, MolecularMolecular StructureSecA ProteinsSEC Translocation ChannelsAdenosine TriphosphatasesAnti-Bacterial AgentsBacterial ProteinsEnzyme InhibitorsMembrane Transport ProteinsSecA ProteinsSEC Translocation Channels

Identifiers

PMID26062397
PMCPMC4479503
OpenAlexW2185851435

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.