DocumentCode :
2528584
Title :
Analysis of four different sets of predictive features for metalloproteins
Author :
Seker, Huseyin ; Haris, Parvez I.
Author_Institution :
Bio-Health Informatics Res. Group, De Montfort Univ., Leicester, UK
fYear :
2005
fDate :
8-11 Aug. 2005
Firstpage :
228
Lastpage :
229
Abstract :
Metals bound to the protein are important for functional or structural roles. Despite their importance there is a distinct lack of research for identification of metalloproteins from sequence data and their predictive features that help distinguish them from non-metal binding proteins. In this study, four sets of features were analysed in order to see their ability to distinguish between metal and non-metal binding proteins. The analysis was carried out using a novel fuzzy logic method. The results show that the amino acid composition is more capable of distinguishing metal from non-metal binding proteins, than any of the other three features, yielding a predictive accuracy of 69.4%. Cofactors were the least useful feature for distinguishing metalloproteins. However, better results were obtained when physico-chemical and secondary structure features are used, yielding accuracies of 67.8% and 67.1%, respectively. Although the amino acid composition yields the highest predictive accuracy, considering the number of features, the latter two sets of features may be more appropriate for such analysis.
Keywords :
biology computing; fuzzy logic; molecular biophysics; proteins; amino acid composition; fuzzy logic method; metal binding proteins; metal bound; metalloproteins; physico-chemical structure; protein; sequence data; Accuracy; Amino acids; Bioinformatics; Biological systems; Biomedical informatics; Computational intelligence; Fuzzy logic; Fuzzy sets; Proteins; Robustness;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Computational Systems Bioinformatics Conference, 2005. Workshops and Poster Abstracts. IEEE
Print_ISBN :
0-7695-2442-7
Type :
conf
DOI :
10.1109/CSBW.2005.23
Filename :
1540610
Link To Document :
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