Evidence map›Paper›PMID 30958095›Full record

ArticleEmerging microbes & infections2019

Genetic and biochemical characterizations of Zika virus NS2A protein.

Xianwen Zhang, Xuping Xie, Jing Zou, Hongjie Xia, Chao Shan, Xinwen Chen, Pei-Yong Shi

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.9field-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

31 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  7. Review
  8. Article
  9. Envelope Protein-Targeting Zika Virus Entry Inhibitors.International journal of molecular sciences · 2024
    Review
  10. Zika Virus Neuropathogenesis-Research and Understanding.Pathogens (Basel, Switzerland) · 2024
    Review
  11. Article
  12. Review
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  15. Review
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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

7 authors at 2 institutions in 2 countries.

Xianwen Zhanga State Key Laboratory of Virology , Wuhan Institute of Virology, Chinese Academy of Sciences , Wuhan , People's Republic of China.
Xuping Xiec Department of Biochemistry & Molecular Biology , University of Texas Medical Branch , Galveston , TX , USA.
Jing Zouc Department of Biochemistry & Molecular Biology , University of Texas Medical Branch , Galveston , TX , USA.
Hongjie Xiac Department of Biochemistry & Molecular Biology , University of Texas Medical Branch , Galveston , TX , USA.
Chao Shanc Department of Biochemistry & Molecular Biology , University of Texas Medical Branch , Galveston , TX , USA.
Xinwen Chena State Key Laboratory of Virology , Wuhan Institute of Virology, Chinese Academy of Sciences , Wuhan , People's Republic of China.
Pei-Yong Shic Department of Biochemistry & Molecular Biology , University of Texas Medical Branch , Galveston , TX , USA.
The University of Texas Medical Branch at Galveston · USWuhan Institute of Virology · CN

Funding

Project 4 - Influenza - UABU19AI142759 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WHITLEY, RICHARD J. · 2019 to 2023
$37.5M
NIAID NIH HHS U19 AI142759
6 · The paper itself

Abstract

Zika virus (ZIKV) can cause devastating congenital Zika syndromes in pregnant women and Guillain-Barre syndrome in adults. Understanding the molecular mechanism of ZIKV replication is essential for antiviral and vaccine development. Here we report the structural and functional characterization of ZIKV NS2A protein. Biochemical structural probing suggests that ZIKV NS2A has a single segment that traverses the ER membrane and six segments that peripherally associate with the ER membrane. Functional analysis has defined distinct NS2A residues essential for viral RNA synthesis or virion assembly. Only the virion assembly-defective mutants, but not the RNA synthesis-defective mutants, could be rescued through trans complementation with a wide-type NS2A protein. These results suggest that the NS2A molecules in virion assembly complex could be recruited in trans, whereas the NS2A molecules in viral replication complex must be recruited in cis. Together with previous results, we propose a flavivirus assembly model where NS2A plays a central role in modulating viral structural and nonstructural proteins as well as genomic RNA during virion assembly.

Indexed as

Cell LineEndoplasmic ReticulumHumansViral Nonstructural ProteinsVirus AssemblyVirus ReplicationZika VirusZika Virus InfectionViral Nonstructural Proteinsflavivirus NS2Aflavivirus replicationmembrane topologyvirion assemblyZika virus

Identifiers

PMID30958095
PMCPMC6455252
OpenAlexW2936936485

What OpenQuestion holds

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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.