Characterization of Proteins from Putative Human DNA and RNA Viruses

Author:

Polanco Carlos1,Uversky Vladimir N.2,Vargas-Alarcón Gilberto3,Buhse Thomas4,Huberman Alberto5,Márquez Manlio F.6,Andrés Leire7

Affiliation:

1. Department of Electromechanical Instrumentation, Instituto Nacional de Cardiología “ Ignacio Chávez”, México City 14800, México | Department of Mathematics, Faculty of Sciences, Universidad Nacional Autónoma de México, México City 04510, México

2. Department of Molecular Medicine and USF Health Byrd Alzheimer\'s Research Institute, Morsani College of Medicine, University of South Florida, Tampa, FL33647, USA | Protein Research Group, Institute for Biological Instrumentation of the Russian Academy of Sciences, Federal Research Center “Pushchino Scientific Center for Biological Research of the Russian Academy of Sciences”, 142290 Pushchino, Moscow region, Russia

3. Research Center, Instituto Nacional de Cardiología “Ignacio Chávez”, México City 14800, México

4. Chemical Research Center, Universidad Autónoma del Estado de Morelos, Cuernavaca Morelos 62209, México

5. Department of Biochemistry, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, C.P. 14080 México City, México

6. Clinical Research Center, Instituto Nacional de Cardiología “Ignacio Chávez”, México City 14800, México

7. Department of Pathology, Hospital de Cruces, 48903, Barakaldo, Spain

Abstract

Background: In the vast variety of viruses known, there is a particular interest in those transmitted to humans and whose ability to disseminate represents a significant public health issue. Objective: The present study’s objective is to bioinformatically characterize the proteins of the two main divisions of viruses, RNA-viruses and DNA-viruses. Methods: In this work, a set of in-house computational programs was used to calculate the polarity/charge profiles and intrinsic disorder predisposition profiles of the proteins of several groups of viruses representing both types extracted from UniProt database. The efficiency of these computational programs was statistically verified. Results: It was found that the polarity/charge profile of the proteins is, in most cases, an efficient discriminant that allows the re-creation of the taxonomy known for both viral groups. Additionally, the entire set of "reviewed" proteins in UniProt database was analyzed to find proteins with the polarity/charge profiles similar to those obtained for each viral group. This search revealed a substantial number of proteins with such polarity-charge profiles. Conclusion: Polarity/charge profile represents a physicochemical metric, which is easy to calculate, and which can be used to effectively identify viral groups from their protein sequences.

Publisher

Bentham Science Publishers Ltd.

Subject

Molecular Biology,Biochemistry

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