Evidence map›Paper›PMID 39248490›Full record

ArticleJournal of virology2024

Identification of amino acid residue in the

Moosung Kim, Minsik Kim, Sangryeol Ryu

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Moosung Kim *Department of Food and Animal Biotechnology, College of Agriculture and Life Sciences, Seoul National University, Seoul, Republic of Korea.ORCID 0009-0000-2613-5112
Minsik Kim *Department of Food and Nutrition, College of Human Ecology, Yonsei University, Seoul, Republic of Korea.ORCID 0000-0003-4133-5600
Sangryeol RyuDepartment of Food and Animal Biotechnology, College of Agriculture and Life Sciences, Seoul National University, Seoul, Republic of Korea.ORCID 0000-0001-5812-3394

Funding

National Research Foundation of Korea (NRF) NRF-2023R1A2C1006359
6 · The paper itself

Abstract

Polyvalent bacteriophages show the feature of infecting bacteria across multiple species or even orders. Infectivity of a polyvalent phage is variable depending on the host bacteria, which can disclose differential inhibition of bacteria by the phage. In this study, a polyvalent phage CSP1 infecting both IMPORTANCE: Polyvalent phages have the advantage of a broader host range, overcoming the limitation of the narrow host range of phages. However, the limited molecular biological understanding on the host bacteria-polyvalent phage interaction hinders its effective application. Here, we revealed that the ability of the polyvalent phage CSP1 to infect

Indexed as

ColiphagesCronobacter sakazakiiEscherichia coliLipopolysaccharidesAmino AcidsEscherichia coli ProteinsHost SpecificityReceptors, VirusVirus AttachmentAmino AcidsEscherichia coli ProteinsLipopolysaccharidesReceptors, VirusLamBlipopolysaccharidepolyvalent bacteriophagereceptorreceptor binding protein

Identifiers

PMID39248490
PMCPMC11494877

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.