Evidence map›Paper›PMID 32209293›Full record

ReviewBioorganic & medicinal chemistry letters2020

The signal peptide as a new target for drug design.

Liezel A Lumangtad, Thomas W Bell

Abstract readReview
In one paragraph

Review in Bioorganic & medicinal chemistry letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Structural Features of a Tiny Viral Protein, ORF7b of SARS-CoV-2.International journal of molecular sciences · 2026
    Article
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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  12. Article
  13. Cell death signaling inExperimental biology and medicine (Maywood, N.J.) · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

2 authors.

Liezel A LumangtadDepartment of Chemistry, University of Nevada, Reno, NV 89557-0216, USA.
Thomas W BellDepartment of Chemistry, University of Nevada, Reno, NV 89557-0216, USA. Electronic address: twb@unr.edu.

Funding

Small-molecule Inhibitors of Human CD4 ExpressionR15GM120659 · NIGMS · UNIVERSITY OF NEVADA RENO · PI BELL, THOMAS W. · 2016 to 2016
$423k
NIGMS NIH HHS R15 GM120659
6 · The paper itself

Abstract

Many current and potential drug targets are membrane-bound or secreted proteins that are expressed and transported via the Sec61 secretory pathway. They are targeted to translocon channels across the membrane of the endoplasmic reticulum (ER) by signal peptides (SPs), which are temporary structures on the N-termini of their nascent chains. During translation, such proteins enter the lumen and membrane of the ER by a process known as co-translational translocation. Small molecules have been found that interfere with this process, decreasing protein expression by recognizing the unique structures of the SPs of particular proteins. The SP may thus become a validated target for designing drugs for numerous disorders, including certain hereditary diseases.

Indexed as

Drug DesignProtein Sorting SignalsAdaptor Proteins, Vesicular TransportCD4 AntigensEndoplasmic ReticulumHumansProtein TransportSmall Molecule LibrariesSortilinAdaptor Proteins, Vesicular TransportCD4 AntigensProtein Sorting SignalsSmall Molecule LibrariesSortilinCADACD4ERHereditary diseasesInhibitorProteinSec61Signal peptideSortilinTranslocation

Identifiers

PMID32209293
PMCPMC7138182

What OpenQuestion holds

Textmetadata
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.