Evidence map›Paper›PMID 29023605›Full record

ArticlePloS one2017

Involvement of the Arg566 residue of Aeromonas sobria serine protease in substrate specificity.

Hidetomo Kobayashi, Tadamune Otsubo, Fumiteru Teraoka, Kiyoshi Ikeda, Soshi Seike, Eizo Takahashi, Keinosuke Okamoto, Toru Yoshida, Hideaki Tsuge, Hiroyasu Yamanaka

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. 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
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Journal of bacteriology · 2026
    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

10 authors at 3 institutions in 2 countries.

Hidetomo KobayashiLaboratory of Molecular Microbiological Science, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
Tadamune OtsuboLaboratory of Synthetic Organic Chemistry, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
Fumiteru TeraokaLaboratory of Synthetic Organic Chemistry, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
Kiyoshi IkedaLaboratory of Synthetic Organic Chemistry, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
Soshi SeikeLaboratory of Molecular Microbiological Science, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
Eizo TakahashiCollaborative Research Center of Okayama University for Infectious Diseases in India, National Institute of Cholera Enteric Diseases JICA Building ID Hospital Campus, Kolkata, India.
Keinosuke OkamotoCollaborative Research Center of Okayama University for Infectious Diseases in India, National Institute of Cholera Enteric Diseases JICA Building ID Hospital Campus, Kolkata, India.
Toru YoshidaDepartment of Bioresource and Environmental Sciences, Faculty of Life Sciences, Kyoto Sangyo University, Kyoto, Japan.
Hideaki TsugeDepartment of Bioresource and Environmental Sciences, Faculty of Life Sciences, Kyoto Sangyo University, Kyoto, Japan.
Hiroyasu YamanakaLaboratory of Molecular Microbiological Science, Faculty of Pharmaceutical Sciences, Hiroshima International University, Hiroshima, Japan.
Hiroshima International University · JPKyoto Sangyo University · JPNational Institute of Cholera and Enteric Diseases · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aeromonas sobria serine protease (ASP) is an extracellular serine protease secreted by the organism. Here, we identified the amino acid residue of ASP that contributes to substrate specificity by using both synthetic peptides and biological protein components. The results showed that the arginine residue at position 566 (Arg-566) of ASP, which is located in the extra occluding region of ASP close to an entrance of the catalytic cavity, is involved in the substrate specificity. A substitutional point mutation of the Arg-566 residue of ASP to Ala residue (ASP[R566A]) caused a decrease of the proteolytic efficiency for a certain substrate. In addition, ASP lost the ability to recognize the primary substrate by such a point mutation, and ASP[R566A] reacted to a wide range of synthetic substrates. It is likely that Arg-566 causes an interaction with the amino acid residue at position P3 of the substrate, which is the third amino acid residue upstream from the cleavage site. Another study using ORF2 protein, a chaperone protein of ASP, further suggested that Arg-566 could also play an important role in interaction with ORF2. We therefore conclude that the Arg-566 residue of ASP is likely responsible for the selection of substrates.

Indexed as

AeromonasAmino Acid SequenceArginineBacterial ProteinsFibrinogenHumansKininogensMolecular ChaperonesMutagenesis, Site-DirectedProteolysisSerine ProteasesSubstrate SpecificityArginineBacterial ProteinsFibrinogenKininogensMolecular ChaperonesSerine Proteases

Identifiers

PMID29023605
PMCPMC5638518
OpenAlexW2763061482

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.