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Protein sequence motifs information is crucial to the analysis of biologically significant regions. The conserved regions have the potential to determine the role of the proteins. Many algorithms or techniques to discover motifs require a predefined fixed window size in advance. Due to the fixed size, these approaches often deliver a number of similar motifs simply shifted by some bases or including...
Protein sequence motifs information is crucial to the analysis of biologically significant regions. The conserved regions have the potential to determine the role of the proteins. Many algorithms or techniques to discover motifs require a predefined fixed window size in advance. Due to the fixed size, these approaches often deliver a number of similar motifs simply shifted by some bases or including...
Protein sequence motifs are gathering more and more attention in the sequence analysis area. These recurring regions have the potential to determine protein 's conformation, function and activities. In our previous work, we tried to obtain protein sequence motifs which are universally conserved across protein family boundaries. Therefore, unlike most popular motif discovering algorithms, our input...
Protein sequence motifs are gathering more and more attention in the sequence analysis area. These recurring regions have the potential to determine protein's conformation, function and activities. In our previous work, we tried to obtain protein sequence motifs which are universally conserved across protein family boundaries. Therefore, unlike most popular motif discovering algorithms, our input...
Protein sequence motifs information is very important to the analysis of biologically significant regions. The conserved regions have the potential to determine the conformation, function and activities of the proteins. The main purpose of this paper is trying to obtain protein sequence motifs which are universally conserved and across protein family boundaries. Therefore, unlike most popular motif...
The microscale techniques of CZE, cIEF and SDS capillary electrophoresis have been evaluated for the analysis of a complex glycoprotein, recombinant tissue plasminogen activator (rtPA). A series of ω-amino acid buffers (pH 5) was found suitable for the CZE separation of rtPA on coated capillaries. rtPA could be resolved into a series of major and minor peaks in an ε-aminocaproic acid buffer containing...
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