Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/77709
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPhasit Charoenkwanen_US
dc.contributor.authorSakawrat Kanthawongen_US
dc.contributor.authorNalini Schaduangraten_US
dc.contributor.authorJanchai Yanaen_US
dc.contributor.authorWatshara Shoombuatongen_US
dc.date.accessioned2022-10-16T08:23:34Z-
dc.date.available2022-10-16T08:23:34Z-
dc.date.issued2020-02-03en_US
dc.identifier.issn20734409en_US
dc.identifier.other2-s2.0-85081155856en_US
dc.identifier.other10.3390/cells9020353en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081155856&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/77709-
dc.description.abstractAlthough, existing methods have been successful in predicting phage (or bacteriophage) virion proteins (PVPs) using various types of protein features and complex classifiers, such as support vector machine and naïve Bayes, these two methods do not allow interpretability. However, the characterization and analysis of PVPs might be of great significance to understanding the molecular mechanisms of bacteriophage genetics and the development of antibacterial drugs. Hence, we herein proposed a novel method (PVPred-SCM) based on the scoring card method (SCM) in conjunction with dipeptide composition to identify and characterize PVPs. In PVPred-SCM, the propensity scores of 400 dipeptides were calculated using the statistical discrimination approach. Rigorous independent validation test showed that PVPred-SCM utilizing only dipeptide composition yielded an accuracy of 77.56%, indicating that PVPred-SCM performed well relative to the state-of-the-art method utilizing a number of protein features. Furthermore, the propensity scores of dipeptides were used to provide insights into the biochemical and biophysical properties of PVPs. Upon comparison, it was found that PVPred-SCM was superior to the existing methods considering its simplicity, interpretability, and implementation. Finally, in an effort to facilitate high-throughput prediction of PVPs, we provided a user-friendly web-server for identifying the likelihood of whether or not these sequences are PVPs. It is anticipated that PVPred-SCM will become a useful tool or at least a complementary existing method for predicting and analyzing PVPs.en_US
dc.subjectMedicineen_US
dc.titlePVPred-SCM: Improved Prediction and Analysis of Phage Virion Proteins Using a Scoring Card Methoden_US
dc.typeJournalen_US
article.title.sourcetitleCellsen_US
article.volume9en_US
article.stream.affiliationsChiang Mai Rajabhat Universityen_US
article.stream.affiliationsKhon Kaen Universityen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.