Interactions between the aromatic amino acid residues have a significant influence on the protein structures and protein-DNA
complexes. These interactions individually provide little stability to the structure; however, together they contribute significantly to
the conformational stability of the protein structure. In this study, we focus on the four aromatic amino acid residues and their
interactions with one another and their individual interactions with the four nucleotide bases. These are analyzed in order to
determine the extent to which their orientation and the number of interactions contribute to the protein and protein-DNA complex
structures.
Various types of sequences in the human genome are known to play important roles in different aspects of genomic functioning.
Among these sequences, palindromic nucleic acid sequences are one such type that have been studied in detail and found to
influence a wide variety of genomic characteristics. For a nucleotide sequence to be considered as a palindrome, its complementary
strand must read the same in the opposite direction. For example, both the strands i.e the strand going from 5' to 3' and its
complementary strand from 3' to 5' must be complementary. A typical nucleotide palindromic sequence would be TATA (5' to 3')
and its complimentary sequence from 3' to 5' would be ATAT. Thus, a new method has been developed using dynamic
programming to fetch the palindromic nucleic acid sequences. The new method uses less memory and thereby it increases the
overall speed and efficiency. The proposed method has been tested using the bacterial (3891 KB bases) and human chromosomal
sequences (Chr-18: 74366 kb and Chr-Y: 25554 kb) and the computation time for finding the palindromic sequences is in milli
seconds.
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