Evidence map›Paper›PMID 25673704›Full record

ArticleJournal of virology2015

A triple-arginine motif in the amino-terminal domain and oligomerization are required for HIV-1 inhibition by human MX2.

Caroline Goujon, Rebecca A Greenbury, Stelios Papaioannou, Tomas Doyle, Michael H Malim

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Article
  3. MX2 Mediates Collapse of the HIV-1 Capsid.bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
  5. Article
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  7. Article
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  10. Review
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  14. Article
  15. Virus-Induced Membrane Fusion in Neurodegenerative Disorders.Frontiers in cellular and infection microbiology · 2022
    Review
  16. Review
  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

5 authors at 1 institution in 1 country.

Caroline GoujonDepartment of Infectious Diseases, King's College London, London, United Kingdom cgoujon@cpbs.cnrs.fr michael.malim@kcl.ac.uk.
Rebecca A GreenburyDepartment of Infectious Diseases, King's College London, London, United Kingdom.
Stelios PapaioannouDepartment of Infectious Diseases, King's College London, London, United Kingdom.
Tomas DoyleDepartment of Infectious Diseases, King's College London, London, United Kingdom.
Michael H MalimDepartment of Infectious Diseases, King's College London, London, United Kingdom cgoujon@cpbs.cnrs.fr michael.malim@kcl.ac.uk.
King's College London · GB

Funding

Department of HealthMedical Research Council G1000196Medical Research Council G1001081Medical Research Council MR/M001199/1Wellcome Trust
6 · The paper itself

Abstract

We have employed molecular genetic approaches to understand the domain organization of the HIV-1 resistance factor myxovirus resistance 2 (MX2). First, we describe an essential triple-arginine motif in the amino-terminal domain. Second, we demonstrate that this 91-residue domain mediates antiviral activity when appended to heterologous proteins, and we provide genetic evidence that protein oligomerization is required for MX2 function. These insights will facilitate future work aiming to elucidate MX2's mechanism of action.

Indexed as

Amino Acid MotifsArginineFlow CytometryFluorescent Antibody Technique, IndirectHIV-1HumansImmunoblottingMolecular Sequence DataMyxovirus Resistance ProteinsPolymerizationArginineMX2 protein, humanMyxovirus Resistance Proteins

Identifiers

PMID25673704
PMCPMC4442396
OpenAlexW2033162292

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.