Evidence map›Paper›PMID 34938415›Full record

ArticleComputational and structural biotechnology journal2021

MutTMPredictor: Robust and accurate cascade XGBoost classifier for prediction of mutations in transmembrane proteins.

Fang Ge, Yi-Heng Zhu, Jian Xu, Arif Muhammad, Jiangning Song, Dong-Jun Yu

Open access · goldAbstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 31 citations in OpenAlex.

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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

6 authors at 2 institutions in 3 countries.

Fang GeSchool of Computer Science and Engineering, Nanjing University of Science and Technology, 200 Xiaolingwei, Nanjing 210094, China.
Yi-Heng ZhuSchool of Computer Science and Engineering, Nanjing University of Science and Technology, 200 Xiaolingwei, Nanjing 210094, China.
Jian XuSchool of Computer Science and Engineering, Nanjing University of Science and Technology, 200 Xiaolingwei, Nanjing 210094, China.
Arif MuhammadSchool of Computer Science and Engineering, Nanjing University of Science and Technology, 200 Xiaolingwei, Nanjing 210094, China.
Jiangning SongMonash Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia.
Dong-Jun YuSchool of Computer Science and Engineering, Nanjing University of Science and Technology, 200 Xiaolingwei, Nanjing 210094, China.
Nanjing University of Science and Technology · CNMonash University · AU

Funding

New Tricks for 'Old' Drugs: PK/PD of Polymyxin Nonantibiotic CombinationsR01AI111965 · NIAID · MONASH UNIVERSITY · PI LI, JIAN · 2014 to 2018
$4.3M
NIAID NIH HHS R01 AI111965
6 · The paper itself

Abstract

Transmembrane proteins have critical biological functions and play a role in a multitude of cellular processes including cell signaling, transport of molecules and ions across membranes. Approximately 60% of transmembrane proteins are considered as drug targets. Missense mutations in such proteins can lead to many diverse diseases and disorders, such as neurodegenerative diseases and cystic fibrosis. However, there are limited studies on mutations in transmembrane proteins. In this work, we first design a new feature encoding method, termed weight attenuation position-specific scoring matrix (WAPSSM), which builds upon the protein evolutionary information. Then, we propose a new mutation prediction algorithm (cascade XGBoost) by leveraging the idea learned from consensus predictors and gcForest. Multi-level experiments illustrate the effectiveness of WAPSSM and cascade XGBoost algorithms. Finally, based on WAPSSM and other three types of features, in combination with the cascade XGBoost algorithm, we develop a new transmembrane protein mutation predictor, named MutTMPredictor. We benchmark the performance of MutTMPredictor against several existing predictors on seven datasets. On the 546 mutations dataset, MutTMPredictor achieves the accuracy (

Indexed as

1000 Genomes, 1000 genomes project consortiumAPOGEE, pathogenicity prediction through the logistic model treeBorodaTM, boosted regression trees for disease-associated mutations in transmembrane proteinsCascade XGBoostClinVar, clinical variantsCondel, consensus deleteriousness score of missense mutationsCOSMIC, catalogue of somatic mutations in cancerDisease-associated mutationsEntprise, entropy and predicted protein structureExAC, the exome aggregation consortiumfathmm, functional analysis through hidden markov modelshumsavar, human polymorphisms and disease mutationsMeta-SNP, meta single nucleotide polymorphismMutation predictionPolyPhen-2, polymorphism phenotyping v2PolyPhen, polymorphism phenotypingPredictSNP1, predict single nucleotide polymorphism v1Pred-MutHTP, prediction of mutations in human transmembrane proteinsProtein evolutionary informationPROVEAN, protein variation effect analyzerREVEL, rare exome variant ensemble learnerSDM, site-directed mutateSIFT, sorting intolerant from tolerantSNAP, screening for non-acceptable polymorphismsSNP&GO, single nucleotide polymorphisms and gene ontology annotationsSwissVar, variants in UniProtKB/Swiss-ProtTMSNP, transmembrane single nucleotide polymorphismsTransmembrane proteinWEKA, waikato environment for knowledge analysis

Identifiers

PMID34938415
PMCPMC8649221
OpenAlexW3216625938

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.