Comprehensive Analysis of Homologous Proteins for Specific Drug Design

Journal Title: STAR Journal - Year 2014, Vol 3, Issue 2

Abstract

A drug is a chemical substance used in the diagnosis, treatment or prevention of disease or as a component of a medication, should be specific and freedom from side affect. Many issues should be addressed while designing a new drug or improving existing compound. The increase in the interdisciplinary nature of science gives bioinformatics, systems and computational biology, which helps in reducing research and development costs, minimize drug failures by predicting drug efficacy and toxicity. One of the most important pathogenic bacterium is Aeromonas species which causes tissue damage, acute gastroenteritis and neonatal septicemia. Bacterial proteins are the ultimate target to inhibit their growth and these are the executors of cellular function. In related to this we selected four such different proteins Flavohemo protein, Guanylate kinase, Topoisomerase and Oligopeptidase found to be present in both humans and Aeromonas to study the effects of antibiotics through in silico approaches. An attempt has been made to classify the inhibitors as host protein inhibitors or guest protein inhibitors. Finally we conclude that the molecule AgkI5 (2-morpholin-4-yl-thianthren-1-ylpyron-4-one) shown good inhibition with minimum binding energy -9.30, docking energy -10.03, inhibition constant 1.53e-007 and RMS 0.0 against Aeromonas Guanylate kinase [Aeromonas: Modelled] when compared to human Guanylate kinase [PDB ID: 1KJD]. So AgkI5 was predicted as a good antibiotic against Aeromonas Species.

Authors and Affiliations

Bharath BR| Department of Biotechnology, N.M.A.M. Institute of Technology, Nitte– 574 110, Karkala, Karnataka, Indiaو Department of P.G Studies and Research in Biotechnology and Bioinformatics, Kuvempu University, Jnanasahyadri, Shankaraghatta – 577 451, Shimoga, Karnataka, India, Sujata Barangi| Department of Biotechnology, N.M.A.M. Institute of Technology, Nitte– 574 110, Karkala, Karnataka, India, Rajesh KP| Department of P.G Studies and Research in Biotechnology and Bioinformatics, Kuvempu University, Jnanasahyadri, Shankaraghatta – 577 451, Shimoga, Karnataka, India, Chetan DM | Department of P.G Studies and Research in Biotechnology and Bioinformatics, Kuvempu University, Jnanasahyadri, Shankaraghatta – 577 451, Shimoga, Karnataka, India, Manjunatha H| Department of P.G Studies and Research in Biotechnology and Bioinformatics, Kuvempu University, Jnanasahyadri, Shankaraghatta – 577 451, Shimoga, Karnataka, India

Keywords

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  • EP ID EP9650
  • DOI http://dx.doi.org/10.4314/star.v3i2.7
  • Views 337
  • Downloads 13

How To Cite

Bharath BR, Sujata Barangi, Rajesh KP, Chetan DM, Manjunatha H (2014). Comprehensive Analysis of Homologous Proteins for Specific Drug Design. STAR Journal, 3(2), 47-62. https://europub.co.uk/articles/-A-9650