Evidence map›Paper›PMID 26329395›Full record

ReviewCritical reviews in biochemistry and molecular biology2015

Manipulation of the host protein acetylation network by human immunodeficiency virus type 1.

Mark Y Jeng, Ibraheem Ali, Melanie Ott

Abstract readReview
In one paragraph

Review in Critical reviews in biochemistry and molecular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. In silico investigation of the viroporin E as a vaccine target against SARS-CoV-2.American journal of physiology. Lung cellular and molecular physiology · 2021
    Article
  7. Review
  8. Article
  9. Targeting HIV-1 proviral transcription.Current opinion in virology · 2019
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Cancer therapies in HIV cure research.Current opinion in HIV and AIDS · 2017
    Review
  15. A Roadmap for Tick-Borne Flavivirus Research in the "Omics" Era.Frontiers in cellular and infection microbiology · 2017
    Review
  16. 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

3 authors at 1 institution in 1 country.

Mark Y Jenga Gladstone Institute of Virology and Immunology , San Francisco , CA , USA and.
Ibraheem Alia Gladstone Institute of Virology and Immunology , San Francisco , CA , USA and.
Melanie Otta Gladstone Institute of Virology and Immunology , San Francisco , CA , USA and.
Gladstone Institutes · US

Funding

Virology CoreP30AI027763 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEVEN Grant DEEKS · 1988 to 2026
$93.6M
Using NK Cells to eliminate the latent HIV reservoirU19AI096113 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LUCIW, PAUL · 2011 to 2015
$39.5M
MOLECULAR AND CELLULAR IMMUNOLOGYT32AI007334 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CYSTER, JASON G · 1988 to 2023
$11.0M
A new model of accelerated immune aging in HIV-infected drug usersDP1DA038043 · NIDA · J. DAVID GLADSTONE INSTITUTES · PI OTT, MELANIE MARIA · 2014 to 2019
$4.8M
Role of Factor Acetylation in the Regulation of HIV TranscriptionR01AI083139 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI OTT, MELANIE MARIA · 2009 to 2017
$3.9M
NIAID NIH HHS P30 AI027763NIAID NIH HHS R01 AI083139NIAID NIH HHS R01AI083139NIAID NIH HHS T32 AI007334NIAID NIH HHS U19 AI096113NIAID NIH HHS U19 AI096113NIDA NIH HHS DP1 DA038043PHS HHS 2 T32 IA 7334-26
6 · The paper itself

Abstract

Over the past 15 years, protein acetylation has emerged as a globally important post-translational modification that fine-tunes major cellular processes in many life forms. This dynamic regulatory system is critical both for complex eukaryotic cells and for the viruses that infect them. HIV-1 accesses the host acetylation network by interacting with several key enzymes, thereby promoting infection at multiple steps during the viral life cycle. Inhibitors of host histone deacetylases and bromodomain-containing proteins are now being pursued as therapeutic strategies to enhance current antiretroviral treatment. As more acetylation-targeting compounds are reaching clinical trials, it is time to review the role of reversible protein acetylation in HIV-infected CD4(+) T cells.

Indexed as

Host-Pathogen InteractionsModels, ImmunologicalProtein Processing, Post-TranslationalAcetylationAnti-HIV AgentsCD4-Positive T-LymphocytesEnzyme InhibitorsHistone AcetyltransferasesHistone Deacetylase InhibitorsHistone DeacetylasesHistonesHIV-1HIV InfectionsHumansIsoenzymesAnti-HIV AgentsEnzyme InhibitorsHistone AcetyltransferasesHistone Deacetylase InhibitorsHistone DeacetylasesHistonesIsoenzymesEpigenetic regulationlatencypost-translational modificationtherapeutic inhibitorsviral infectionvirus–host interactions

Identifiers

PMID26329395
PMCPMC4816045
OpenAlexW2167549252

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.