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Please use this identifier to cite or link to this item: http://ntour.ntou.edu.tw:8080/ir/handle/987654321/27885

Title: Unique Peptide Identification of RNaseA Superfamily Sequences based on Reinforced Merging Algorithms
Authors: Tun-Wen Pai;Bo-Han Su;Pei-Chih Wu;Margaret Dah-Tsyr Chang;Hao-Teng Chang;Tan-Chi Fan;Shi-Hwei Liu
Contributors: NTOU:Department of Computer Science and Engineering
國立臺灣海洋大學:資訊工程學系
Keywords: unique peptide;ribonuclease A superfamily;reinforced merging algorithm
Date: 2006-02
Issue Date: 2011-10-21T02:34:20Z
Publisher: Journal of Bioinformatics and Computational Biology
Abstract: Abstract:Human ribonuclease A (RNaseA) superfamily consists of eight RNases with high similarity in which RNase2 and RNase3 share 76.7% identity. The evolutionary variation of RNases results in differential structures and functions of the enzymes. To distinguish the characteristics of each RNase, we developed reinforced merging algorithms (RMA) to rapidly identify the unique peptide motifs for each member of the highly conserved human RNaseA superfamily. Many motifs in RNase3 identified by RMA correlated well with the antigenic regions predicted by DNAStar. Two unique peptide motifs were experimentally confirmed to contain epitopes for monoclonal antibodies (mAbs) specifically against RNase3. Further analysis of homologous RNases in different species revealed that the unique peptide motifs were located at the correspondent positions, and one of these motifs indeed matched the epitope for a specific anti-bovine pancreatic RNaseA (bpRNaseA) antibody. Our method provides a useful tool for identification of unique peptide motifs for further experimental design. The RMA system is available and free for academic use at http://bioinfo.life.nthu.edu.tw/rma/ and http://spider.cs.ntou.edu.tw/bioinformatics/RMA.html.
Relation: 4(1), pp.75-92
URI: http://ntour.ntou.edu.tw/handle/987654321/27885
Appears in Collections:[資訊工程學系] 期刊論文

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