Treponema pallidum, a Gram negative bacterium, causes chronic disease syphilis, a sexually transmitted disease.
T. pallidum penetrates dermal micro abrasions or intact mucous membranes resulting in varieties of symptoms. The
complete genome for T. pallidum was sequenced, which contains approximately 1,090 genes encoding approximately
1,041 proteins. These open reading frames account for a large number of hypothetical proteins (HPs) for which no pieces
of experimental evidence are available. Being a virulent and not very well characterized organism, it is essential to analyze
these HPs whose structure and function are not available in the protein data bank. Here, our aim is to predict structure
and ultimately function of HPs using combination of modern bioinformatics tools. We successfully modeled the structures
of six HPs with high accuracy, which possess endonuclease, NTP-transferase, transcription regulator and DNA-binding
activities. We further performed virulence search to check their potential role in pathogenicity. Here, we performed an extensive
structure analysis to get an insight into the function of a particular HP. We believe that these analyses expand our
knowledge regarding the functional roles of HPs in the T. pallidum and provide an opportunity to validate novel potential
Homology modeling, sequence analysis, structural genomics, treponema pallidum, virulence factor and function
Center for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, Jamia Nagar, New Delhi – 110025, India.