Evidence map›Paper›PMID 28096973›Full record

ArticleCell & bioscience2017

A fission yeast cell-based system for multidrug resistant HIV-1 proteases.

Zsigmond Benko, Dong Liang, Ge Li, Robert T Elder, Anindya Sarkar, Jun Takayama, Arun K Ghosh, Richard Y Zhao

Open access · goldAbstract read
In one paragraph

Article in Cell & bioscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. An "In Schizo" Evaluation System to Screen for Human Kinesin-5 Inhibitors.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Yeast for virus research.Microbial cell (Graz, Austria) · 2017
    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

8 authors at 3 institutions in 2 countries.

Zsigmond BenkoDepartment of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201 USA ; Department of Membrane Biochemistry, Institute of Animal Biochemistry and Genetics, Centre of Biosciences, SAS, 84005 Bratislava, Slovakia.
Dong LiangDepartment of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201 USA.
Ge LiDepartment of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201 USA.
Robert T ElderChildren's Memorial Institute for Education and Research, Northwestern University Feinberg School of Medicine, Chicago, IL 10164 USA.
Anindya SarkarDepartment of Chemistry, Purdue University, West Lafayette, IN 47907 USA.
Jun TakayamaDepartment of Chemistry, Purdue University, West Lafayette, IN 47907 USA.
Arun K GhoshDepartment of Chemistry, Purdue University, West Lafayette, IN 47907 USA.
Richard Y ZhaoDepartment of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201 USA ; Department of Microbiology-Immunology, University of Maryland School of Medicine, Baltimore, MD 21201 USA ; Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD 21201 USA ; Children's Memorial Institute for Education and Research, Northwestern University Feinberg School of Medicine, Chicago, IL 10164 USA.ORCID 0000-0003-3424-2852
Purdue University West Lafayette · USUniversity of Maryland, Baltimore · USNorthwestern University · US

Funding

Design & Synthesis of Nonpeptide Protease InhibitorsR37GM053386 · NIGMS · PURDUE UNIVERSITY · PI GHOSH, ARUN K · 2011 to 2018
$3.9M
DESIGN AND SYNTHESIS OF NONPEPTIDE PROTEASE INHIBITORSR01GM053386 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GHOSH, ARUN K · 1995 to 2010
$3.7M
A Novel and High Throughput System for Drug Discovery and Testing on Multidrug Resistant HIV-1 ProteasesR01GM127212 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI ZHAO, RICHARD YUQI · 2017 to 2018
$603k
Fission Yeast as a HTS Platform for New Molecular Probes of HIV-1 VPR-Medicated AR21NS063880 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI ZHAO, RICHARD YUQI · 2008 to 2010
$188k
NIGMS NIH HHS R01 GM053386NIGMS NIH HHS R01 GM127212NIGMS NIH HHS R37 GM053386NINDS NIH HHS R21 NS063880
6 · The paper itself

Abstract

backgroundHIV-1 protease (PR) is an essential enzyme for viral production. Thus, PR inhibitors (PIs) are the most effective class of anti-HIV drugs. However, the main challenge to the successful use of PI drugs in patient treatment is the emergence of multidrug resistant PRs (

resultsThree

conclusionsThe three clinically isolated

Indexed as

Cell deathCell proliferationFission yeastHIV-1MitochondriaMultidrug resistant proteasesOxidative stressProtease inhibitorsProteolytic cleavage

Identifiers

PMID28096973
PMCPMC5225522
OpenAlexW2572410680

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.