2016
DOI: 10.1038/srep38318
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Mal-Lys: prediction of lysine malonylation sites in proteins integrated sequence-based features with mRMR feature selection

Abstract: Lysine malonylation is an important post-translational modification (PTM) in proteins, and has been characterized to be associated with diseases. However, identifying malonyllysine sites still remains to be a great challenge due to the labor-intensive and time-consuming experiments. In view of this situation, the establishment of a useful computational method and the development of an efficient predictor are highly desired. In this study, a predictor Mal-Lys which incorporated residue sequence order informatio… Show more

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Cited by 49 publications
(38 citation statements)
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“…This method is widely recognized in application domains, such as artificial intelligence (AI) algorithms [14], medical disease diagnosis [15], bioengineering [16], and electric engineering [17]. The method has become a much focused classic in the feature selection area given its effectiveness.…”
Section: Introductionmentioning
confidence: 99%
“…This method is widely recognized in application domains, such as artificial intelligence (AI) algorithms [14], medical disease diagnosis [15], bioengineering [16], and electric engineering [17]. The method has become a much focused classic in the feature selection area given its effectiveness.…”
Section: Introductionmentioning
confidence: 99%
“…While these modifications have recently been implicated as important regulators of metabolism, our knowledge regarding their biological significance is still in its infancy 5860 . Malonyl-lysine and succinyllysine modifications induce dramatic structural changes on lysine residues due to their large size and they frequently occur together 61 . Our data are consistent with these previous observations, however, in the context of DBI proteoforms, the biological consequence of these modifications is yet unknown.…”
Section: Discussionmentioning
confidence: 99%
“…AAindex 37 is a database that holds numerous physicochemical and biological properties of amino acids. Several mixtures of physicochemical properties have been employed that effectively convert sequences of peptides into mathematical expressions 18 , 38 40 . In this study, we used 14 physicochemical properties: hydrophobicity, solvent accessibility, polarity, polarizability, accessibility, PK-N , PK-C , melting point, molecular weight, optical rotation, net charge index of side chains, entropy of formation, heat capacity and absolute entropy.…”
Section: Methodsmentioning
confidence: 99%