Thymine is the one and only base transcribed into uracil during production of proteins. Thymine in DNA and uracil in mRNA plays a major role in producing proteins with appropriate carbon content for stability and activity. Thymine distribution is different frames of coding nucleic acids are investigated statistically. The results confirm that frame 1 supposed to have definite thymine content. Frame 3 prefers to have least thymine content. Frames 4 & 5 maintain some degree of thymine while 2 & 6 have a variable fraction of thymine.

Urogenital schistosomiasis is frequently occurring parasitic disease in tropical countries, S. haematobium is main causative agent responcible for urogenital schistosomiasis; till date no effective invention made to against urogenital schistosomiasis. In this analysis we a have predicted suitable antigenic peptides from Schistosoma haematobium 23-kDa transmembrane protein for peptide vaccine design against urogenital schistosomiasis based on cross protection phenomenon as, an ample immune response can be generated with a single protein subunit. We found MHC class II binding peptides of S. haematobium 23-kDa are important determinant against the diseased condition. The analysis shows S. haematobium 23-kDa transmembrane protein having 218 amino acids, which shows 210 nonamers. In this assay, we have predicted MHC-I binding peptides for 8mer_H2_Db allele (optimal score is 14.128), 9mer_H2_Db allele (optimal score is 20.065), 10mer_H2_Db allele (optimal score is 13.776), 11mer_H2_Db allele (optimal score is 31.213). We also predicted the SVM based MHCII-IAb peptide regions, 152-DYGPNIPAS, 51-WQAAPIAII, 50-VWQAAPIAI, 142-FHCCGAKGP, 97-AELAAAIVA (optimal score is 14.911); MHCII-IAd peptide regions, 100-AAAIVAVVY, 71-LGCCGAIKE, 192-FGVCFFQLL, 186-IVACVAFGV (optimal score is 13.112); and MHCII-IAg7 peptide regions 42-QYGDNLHKV, 101-AAIVAVVYK, 28-VLIGAGAYV, 103-IVAVVYKDR, 203-VIACCLGRQ (optimal score is 11.605) which shows potential binders from S. haematobium 23-kDa transmembrane protein. The method integrates prediction of MHC class I binding proteasomal C- terminal cleavage peptides and Six potential antigenic peptides at average propensity 1.094 having highest local hydrophilicity. Thus a small antigen fragment can induce immune response against whole antigen. This approach can be applied for designing subunit and synthetic peptide vaccines.