| Literature DB >> 34258737 |
Murugesan Vanangamudi1, Pramod C Nair2, S E Maida Engels3, Senthilkumar Palaniappan4, Vigneshwaran Namasivayam5.
Abstract
Human immunodeficiency virus (HIV) is a deadly virus that attacks the body's immune system, subsequently leading to AIDS (acquired immunodeficiency syndrome) and ultimately death. Currently, there is no vaccine or effective cure for this infection; however, antiretrovirals that act at various phases of the virus life cycle have been useful to control the viral load in patients. One of the major problems with antiretroviral therapies involves drug resistance. The three-dimensional structure from crystallography studies are instrumental in understanding the structural basis of drug binding to various targets. This chapter provides key insights into different targets and drugs used in the treatment from a structural perspective. Specifically, an insight into the binding characteristics of drugs at the active and allosteric sites of different targets and the importance of targeting allosteric sites for design of new-generation antiretrovirals to overcome complex and resistant forms of the virus has been reviewed.Entities:
Keywords: AIDS/HIV; Drug resistance; Entry inhibitors; Integrase inhibitor; Non-nucleoside RT inhibitors; Nucleoside RT inhibitors; Protease inhibitors; X-ray crystallography
Year: 2021 PMID: 34258737 DOI: 10.1007/978-981-16-0267-2_3
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622