Evidence map›Paper›PMID 40391298›Full record

ArticleComputational and structural biotechnology journal2025

Prediction and validation of nanowire proteins in

Dheeraj Raya, Vincent Peta, Alain Bomgni, Shiva Aryal, Tuyen Duc Do, Kalimuthu Jawaharraj, David R Salem, Venkataramana Gadhamshetty, Saurabh Sudha Dhiman, Etienne Z Gnimpieba

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Genome announcement of sulfate-reducingMicrobiology resource announcements · 2026
    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.

Dheeraj RayaCivil and Environmental Engineering, South Dakota Mines, Rapid City, SD 57701, USA.
Vincent PetaData Driven Material Discovery Center for Bioengineering Innovation, South Dakota Mines, Rapid City, SD 57701, USA.
Alain BomgniBiomedical Engineering Department, University of South Dakota, Sioux Falls, SD 57107, USA.
Shiva AryalBiomedical Engineering Department, University of South Dakota, Sioux Falls, SD 57107, USA.
Tuyen Duc DoBiomedical Engineering Department, University of South Dakota, Sioux Falls, SD 57107, USA.
Kalimuthu JawaharrajCivil and Environmental Engineering, South Dakota Mines, Rapid City, SD 57701, USA.
David R SalemChemical and Biological Engineering, South Dakota Mines, Rapid City, SD 57701, USA.
Venkataramana GadhamshettyCivil and Environmental Engineering, South Dakota Mines, Rapid City, SD 57701, USA.
Saurabh Sudha DhimanCivil and Environmental Engineering, South Dakota Mines, Rapid City, SD 57701, USA.
Etienne Z Gnimpieba2Dimensional Materials for Biofilm Engineering, Science and Technology Center, South Dakota Mines, Rapid City, SD 57701, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The type-IV bacterial pili and multiheme c-type cytochrome protein family have gained significant attention due to their role in extracellular electron transfer (EET), which defines their electrogenic properties. These electrogenic behaviors play a crucial role in interspecies microbial communication, essential for microbial biofilm formation and the development of robust technologies such as biosensors. Given the technological and ecological significance of electron transfer mechanisms, this study presents NanowireML (NWML), a 2-staged machine learning (ML) system to identify and analyze nanowire (NW) proteins. Stage 1 predicts NW proteins using minimal features, and Stage 2 leverages graphical knowledge representation to predict the most relevant NW mechanism governing candidates in specific experimental conditions. To train the stage 1 model, we used a comprehensive dataset of 999 proteins from a public database specializing in NW development. The primary objective of the NWML model is to identify and validate microbial proteins involved in the biogenesis of NW. Protein feature, such as dipeptide amino acid composition, transition, and distribution enhance the model's performance. Gene ontology (GO) analysis revealed that NW are structural extrusions, part of membranal proteins, with several exposed metal ion binding motifs. The predicted NW protein collection advances to stage 2, where their GO knowledge is stored using a graphical representation. A customized deep neural network (biologically influenced neural networks: BINN) then predicts the most relevant biological pathways governing NW formation using experimental gene expression data. Our study provides detailed insights into gene sets, unveiling the mechanistic networks and pathways crucial for NW formation. These findings enable data-driven decisions for biomedical and biotechnological applications. The NWML model demonstrated high accuracy achieving 94.87 %, 96.68 %, 96.65 %, 96.05 %, and 96.13 % on support vector machine (SVM), random forest (RF), extreme gradient boosting (XGBoost), logistic regression (LR), and artificial neural network (ANN).

Indexed as

Bacterial nanowiresBiofilmBiologically informed neural networkGene ontologyMachine learningProtein sequence-based predictionRandom forest

Identifiers

PMID40391298
PMCPMC12088768

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.