Evidence map›Paper›PMID 40751592›Full record

ArticleFEBS letters2025

Functional role and folding properties of the glucan-binding domain of oral bacterial glucansucrase.

Hideyuki Komatsu, Takayuki Sadakane, Yudai Murata, Junichi Taira, Hiroshi Sakamoto, Takao Kodama

Abstract read
In one paragraph

Article in FEBS letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing 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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Hideyuki KomatsuDepartment of Bioscience and Bioinformatics, School of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.ORCID https://orcid.org/0000-0002-6630-0036
Takayuki SadakaneDepartment of Bioscience and Bioinformatics, School of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.
Yudai MurataDepartment of Bioscience and Bioinformatics, School of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.
Junichi TairaDepartment of Bioscience and Bioinformatics, School of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.
Hiroshi SakamotoDepartment of Bioscience and Bioinformatics, School of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.
Takao KodamaDepartment of Bioscience and Bioinformatics, School of Computer Science and Systems Engineering, Kyushu Institute of Technology, Fukuoka, Japan.

Funding

Japan Society for the Promotion of Science 13671904Japan Society for the Promotion of Science 13680744
6 · The paper itself

Abstract

A Streptococcus sobrinus glucansucrase (i.e., glucosyltransferase-I) elongates α-1, 3-linked glucose chains at pre-existing branch points of dextran, and its activity is enhanced by primer dextran. The glucansucrase contains a catalytic domain and a glucan-binding domain (GBd) with six tandem repeats. We here examined the role of GBd in the glucansucrase, focusing on its impact on enzymatic activity, dextran binding, and structural stability. By generating seven deletion mutants and a circularly permuted protein, our research demonstrates that the first four tandem repeats in the GBd and proper domain orientation are required for efficient glucosyl transfer. Moreover, characterization of circular dichroism and thermal unfolding indicated that glucosyl transfer efficiency is linked to cooperative interdomain folding. These findings highlight the importance of interdomain allostery in optimizing glucansucrase function. Impact statement Our research on the role of the glucan-binding domain in Streptococcus sobrinus glucansucrase revealed that glucosyl transfer efficiency is linked to cooperative interdomain folding. The finding highlights the importance of interdomain allostery in optimizing glucansucrase function and also suggests potential targets for inhibiting bacterial biofilm formation.

Indexed as

Bacterial ProteinsGlucansGlucosyltransferasesGlycosyltransferasesDextransProtein BindingProtein DomainsProtein FoldingalternansucraseBacterial ProteinsDextransGlucansGlucosyltransferasesGlycosyltransferasescooperative unfoldingdextranglucansucraseinterdomain allosteryprotein–polysaccharide interaction

Identifiers

PMID40751592
PMCPMC12375890

What OpenQuestion holds

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Registered trials

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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.