The purpose of this study is to deal with aetiology causing bovine mastitis; bovine herpes virus
is also responsible for causing bovine mastitis but studies on viruses have been neglected as
historical mastitis research has concentrated only on bacterial pathogens. Therefore, present
study aims to make an in silico identification and characterization of potential drug targets in
bovine herpes virus 4 by computational methods using various bioinformatics tools. In the
current investigation 5 proteins of BoHV 4 were found to be nonhomologous to the host Bos
taurus; these nonhomology proteins were believed to be inevitable proteins of BoHV 4 as they
were specific to the virus; however 378 proteins were homologous to the host protein. The in silico
physicochemical characterization of 5 proteins of BoHV 4 indicated that all the proteins of the virus
were having more or less similar characteristics. Perhaps the knowledge of the present study may
help in drug discovery which have high affinity to target site. Possible drug discovery to manage
bovine mastitis with a help of bioinformatics tool is more significant and, specific and, reduces time and
complications involved in clinical trials.