Results 1 to 10 of about 183,370 (170)

In silico prediction of mutant HIV-1 proteases cleaving a target sequence. [PDF]

open access: yesPLoS ONE, 2014
HIV-1 protease represents an appealing system for directed enzyme re-design, since it has various different endogenous targets, a relatively simple structure and it is well studied. Recently Chaudhury and Gray (Structure (2009) 17: 1636-1648) published a
Jan H Jensen   +3 more
doaj   +10 more sources

HIV Protease: Historical Perspective and Current Research [PDF]

open access: yesViruses, 2021
The retroviral protease of human immunodeficiency virus (HIV) is an excellent target for antiviral inhibitors for treating HIV/AIDS. Despite the efficacy of therapy, current efforts to control the disease are undermined by the growing threat posed by ...
Irene T. Weber   +2 more
doaj   +2 more sources

Susceptibility of HPV-18 Cancer Cells to HIV Protease Inhibitors [PDF]

open access: yesViruses
Cervical cancer cases continue to rise despite all the advanced screening and preventative measures put in place, which include human papillomavirus (HPV) vaccination.
Lilian Makgoo   +2 more
doaj   +2 more sources

Molecular Mechanisms of HIV Protease Inhibitors Against HPV-Associated Cervical Cancer: Restoration of TP53 Tumour Suppressor Activities [PDF]

open access: yesFrontiers in Molecular Biosciences, 2022
Cervical cancer is a Human Papilloma virus-related disease, which is on the rise in a number of countries, globally. Two essential oncogenes, E6 and E7, drive cell transformation and cancer development.
Lilian Makgoo   +2 more
doaj   +2 more sources

HIV protease inhibitors restore amphotericin B activity against Candida. [PDF]

open access: yesPLoS ONE
Candida auris is an invasive fungal pathogen, representing a global public health threat. It is characterized by high mortality rates among infected individuals, significant antifungal resistance, and a remarkable ability to persist in healthcare ...
Yehia Elgammal   +2 more
doaj   +2 more sources

HIV protease cleaves the antiviral m6A reader protein YTHDF3 in the viral particle. [PDF]

open access: yesPLoS Pathogens, 2020
N6-methyladenosine (m6A) is the most abundant HIV RNA modification but the interplay between the m6A reader protein YTHDF3 and HIV replication is not well understood.
Denise Jurczyszak   +9 more
doaj   +2 more sources

Patients with discordant responses to antiretroviral therapy have impaired killing of HIV-infected T cells. [PDF]

open access: yesPLoS Pathogens, 2010
In medicine, understanding the pathophysiologic basis of exceptional circumstances has led to an enhanced understanding of biology. We have studied the circumstance of HIV-infected patients in whom antiretroviral therapy results in immunologic benefit ...
Sekar Natesampillai   +6 more
doaj   +1 more source

Infected cell killing by HIV-1 protease promotes NF-kappaB dependent HIV-1 replication. [PDF]

open access: yesPLoS ONE, 2008
Acute HIV-1 infection of CD4 T cells often results in apoptotic death of infected cells, yet it is unclear what evolutionary advantage this offers to HIV-1.
Gary D Bren   +6 more
doaj   +1 more source

Predicting HIV-1 Protease Cleavage Sites With Positive-Unlabeled Learning

open access: yesFrontiers in Genetics, 2021
Understanding the substrate specificity of HIV-1 protease plays an essential role in the prevention of HIV infection. A variety of computational models have thus been developed to predict substrate sites that are cleaved by HIV-1 protease, but most of ...
Zhenfeng Li   +3 more
doaj   +1 more source

Ultra-fast analysis of plasma and intracellular levels of HIV protease inhibitors in children: a clinical application of MALDI mass spectrometry. [PDF]

open access: yesPLoS ONE, 2010
HIV protease inhibitors must penetrate into cells to exert their action. Differences in the intracellular pharmacokinetics of these drugs may explain why some patients fail on therapy or suffer from drug toxicity.
Jeroen J A van Kampen   +10 more
doaj   +1 more source

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