Results 1 to 10 of about 92,880 (144)

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   +7 more sources

HIV Protease: Historical Perspective and Current Research

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 ...
Robert W Harrison, Irène T Weber
exaly   +3 more sources

A folding inhibitor of the HIV-1 Protease [PDF]

open access: yesProteins: Structure, Function, and Bioinformatics, 2005
Being the HIV-1 Protease (HIV-1-PR) an essential enzyme in the viral life cycle, its inhibition can control AIDS. The folding of single domain proteins, like each of the monomers forming the HIV-1-PR homodimer, is controlled by local elementary ...
Abkevich   +35 more
core   +4 more sources

Molecular Basis for Drug Resistance in HIV-1 Protease

open access: yesViruses, 2010
HIV-1 protease is one of the major antiviral targets in the treatment of patients infected with HIV-1. The nine FDA approved HIV-1 protease inhibitors were developed with extensive use of structure-based drug design, thus the atomic details of how the ...
Akbar Ali, Yufeng Cai, Aysegul Özen
exaly   +3 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

HIV protease inhibitors and obesity [PDF]

open access: yesCurrent Opinion in Endocrinology, Diabetes and Obesity, 2010
To review the current scientific literature and recent clinical trials on HIV protease inhibitors and their potential role in the pathogenesis of lipodystrophy and metabolic disorders.HIV protease inhibitor treatment may affect the normal stimulatory effect of insulin on glucose and fat storage.
Erdembileg, Anuurad   +2 more
openaire   +2 more sources

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

Rapid enzymatic test for phenotypic HIV protease drug resistance [PDF]

open access: yes, 2003
A phenotypic resistance test based on recombinant expression of the active HIV protease in E. coli from patient blood samples was developed. The protease is purified in a rapid onestep procedure as active enzyme and tested for inhibition by five selected
Assfalg-Machleidt, Irmgard   +5 more
core   +1 more source

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