期刊文献+

A Review of Machine Learning and Algorithmic Methods for Protein Phosphorylation Site Prediction

原文传递
导出
摘要 Post-translational modifications(PTMs)have key roles in extending the functional diversity of proteins and,as a result,regulating diverse cellular processes in prokaryotic and eukaryotic organisms.Phosphorylation modification is a vital PTM that occurs in most proteins and plays a significant role in many biological processes.Disorders in the phosphorylation process lead to multiple diseases,including neurological disorders and cancers.The purpose of this review is to organize this body of knowledge associated with phosphorylation site(p-site)prediction to facilitate future research in this field.At first,we comprehensively review all related databases and introduce all steps regarding dataset creation,data preprocessing,and method evaluation in p-site prediction.Next,we investigate p-site prediction methods,which are divided into two computational groups:algorithmic and machine learning(ML).Additionally,it is shown that there are basically two main approaches for p-site prediction by ML:conventional and end-to-end deep learning methods,both of which are given an overview.Moreover,this review introduces the most important feature extraction techniques,which have mostly been used in p-site prediction.Finally,we create three test sets from new proteins related to the released version of the database of protein post-translational modifications(dbPTM)in 2022 based on general and human species.Evaluating online p-site prediction tools on newly added proteins introduced in the dbPTM 2022 release,distinct from those in the dbPTM 2019 release,reveals their limitations.In other words,the actual performance of these online p-site prediction tools on unseen proteins is notably lower than the results reported in their respective research pape.
出处 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2023年第6期1266-1285,共20页 基因组蛋白质组与生物信息学报(英文版)
  • 相关文献

参考文献4

二级参考文献17

  • 1[1]Salway,J.G.1999.Metabolism at a Glance (second editon).Blackwell Publishing Ltd.,Oxford,UK.
  • 2[2]Rang,H.P.,et al.1999.Pharmacology (fourth edition).Churchill Livingstone,Edinburgh,UK.
  • 3[3]Matthews,H.R.1995.Protein kinases and phosphatases that act on histidine,lysine,or arginine residues in eukaryotic proteins:a possible regulator of the mitogen-activated protein kinase cascade.Pharmacol.Ther.67:323-350.
  • 4[4]Hardie,D.G.(ed.) 1999.Protein Phosphorylation:A Practical Approach.Oxford University Press,New York,USA.
  • 5[5]Blom,N.,et al.1999.Sequence and structure-based prediction of eukaryotic protein phosphorylation sites.J.Mol.Biol.294:1351-1362.
  • 6[6]Pinna,L.A.and Ruzzene,M.1996.How do protein kinases recognize their substrates? Biochim.Biophys.Acta 1314:191-225.
  • 7[7]Berry,E.A.,et al.2004.Reduced bio basis function neural network for identification of protein phosphorylation sites:comparison with pattern recognition algorithms.Comput.Biol.Chem.28:75-85.
  • 8[8]Kim,J.H.,et al.2004.Prediction of phosphorylation sites using SVMs.Bioinformatics 20:3179-3184.
  • 9[9]Bagley,S.C.and Altman,R.B.1995.Characterizing the microenvironment surrounding protein sites.Protein Sci.4:622-635.
  • 10[10]Wei,L.and Altman,R.B.1998.Recognizing protein binding sites using statistical descriptions of their 3D environments.Pac.Symp.Biocomput.pp.497-508.

共引文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部