Active human immunodeficiency virus protease is required for viral infectivity
about
Identification and characterization of a novel retroviral-like aspartic protease specifically expressed in human epidermisBile pigments as HIV-1 protease inhibitors and their effects on HIV-1 viral maturation and infectivity in vitroEffect of mutations affecting the p6 gag protein on human immunodeficiency virus particle releaseRole of capsid precursor processing and myristoylation in morphogenesis and infectivity of human immunodeficiency virus type 1A novel self-replicating chimeric lentivirus-like particleActivity of purified biosynthetic proteinase of human immunodeficiency virus on natural substrates and synthetic peptidesThe development of antiretroviral therapy and its impact on the HIV-1/AIDS pandemicCleavage of human and mouse cytoskeletal and sarcomeric proteins by human immunodeficiency virus type 1 protease. Actin, desmin, myosin, and tropomyosinInhibitors of human immunodeficiency virus type 1 zinc fingers prevent normal processing of gag precursors and result in the release of noninfectious virus particlesRationale and clinical utility of the darunavir-cobicistat combination in the treatment of HIV/AIDSCurrent perspectives on HIV-1 antiretroviral drug resistanceInhibition of the HIV-1 and HIV-2 proteases by a monoclonal antibodyCrystal structure of an in vivo HIV-1 protease mutant in complex with saquinavir: Insights into the mechanisms of drug resistance1.9 A x-ray study shows closed flap conformation in crystals of tethered HIV-1 PRDiscovery of MK-8718, an HIV Protease Inhibitor Containing a Novel Morpholine Aspartate Binding GroupEffect of the Active Site D25N Mutation on the Structure, Stability, and Ligand Binding of the Mature HIV-1 ProteaseNinety-Nine Is Not Enough: Molecular Characterization of Inhibitor-Resistant Human Immunodeficiency Virus Type 1 Protease Mutants with Insertions in the Flap RegionEnzymatic and structural analysis of the I47A mutation contributing to the reduced susceptibility to HIV protease inhibitor lopinavirStructure of HIV-1 protease in complex with potent inhibitor KNI-272 determined by high-resolution X-ray and neutron crystallographyMolecular Characterization of Clinical Isolates of Human Immunodeficiency Virus Resistant to the Protease Inhibitor DarunavirCatalytic Water Co-Existing with a Product Peptide in the Active Site of HIV-1 Protease Revealed by X-Ray Structure AnalysisStructural basis of alpha-fucosidase inhibition by iminocyclitols with K(i) values in the micro- to picomolar rangeContribution of the 80s loop of HIV-1 protease to the multidrug-resistance mechanism: crystallographic study of MDR769 HIV-1 protease variantsHydrophobic Core Flexibility Modulates Enzyme Activity in HIV-1 ProteasePotent Antiviral HIV-1 Protease Inhibitor GRL-02031 Adapts to the Structures of Drug Resistant Mutants with Its P1′-Pyrrolidinone RingHIV-1 Protease with 20 Mutations Exhibits Extreme Resistance to Clinical Inhibitors through Coordinated Structural RearrangementsCrystal structures of multidrug-resistant HIV-1 protease in complex with two potent anti-malarial compoundsP2' Benzene Carboxylic Acid Moiety Is Associated with Decrease in Cellular Uptake: Evaluation of Novel Nonpeptidic HIV-1 Protease Inhibitors Containing P2 bis-Tetrahydrofuran MoietyGS-8374, a Prototype Phosphonate-Containing Inhibitor of HIV-1 Protease, Effectively Inhibits Protease Mutants with Amino Acid InsertionsInhibition of XMRV and HIV-1 proteases by pepstatin A and acetyl-pepstatinA Conserved Hydrogen-Bonding Network of P2 bis-Tetrahydrofuran-Containing HIV-1 Protease Inhibitors (PIs) with a Protease Active-Site Amino Acid Backbone Aids in Their Activity against PI-Resistant HIVCarbamylation of N-Terminal ProlineStructural Basis of Why Nelfinavir-Resistant D30N Mutant of HIV-1 Protease Remains Susceptible to SaquinavirABT-538 is a potent inhibitor of human immunodeficiency virus protease and has high oral bioavailability in humansCrystal structure of human immunodeficiency virus (HIV) type 2 protease in complex with a reduced amide inhibitor and comparison with HIV-1 protease structuresThe aspartic proteasesThioltransferase (glutaredoxin) is detected within HIV-1 and can regulate the activity of glutathionylated HIV-1 protease in vitroIn vitro inhibition of human immunodeficiency virus (HIV) type 1 replication by C2 symmetry-based HIV protease inhibitors as single agents or in combinationsHuman immunodeficiency virus type 1 protease inhibitors irreversibly block infectivity of purified virions from chronically infected cellsAntiviral and pharmacokinetic properties of C2 symmetric inhibitors of the human immunodeficiency virus type 1 protease
P2860
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P2860
Active human immunodeficiency virus protease is required for viral infectivity
description
1988 nî lūn-bûn
@nan
1988 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Active human immunodeficiency virus protease is required for viral infectivity
@ast
Active human immunodeficiency virus protease is required for viral infectivity
@en
Active human immunodeficiency virus protease is required for viral infectivity
@nl
type
label
Active human immunodeficiency virus protease is required for viral infectivity
@ast
Active human immunodeficiency virus protease is required for viral infectivity
@en
Active human immunodeficiency virus protease is required for viral infectivity
@nl
prefLabel
Active human immunodeficiency virus protease is required for viral infectivity
@ast
Active human immunodeficiency virus protease is required for viral infectivity
@en
Active human immunodeficiency virus protease is required for viral infectivity
@nl
P2093
P2860
P3181
P356
P1476
Active human immunodeficiency virus protease is required for viral infectivity
@en
P2093
E M Scolnick
J C Heimbach
W A Schleif
P2860
P304
P3181
P356
10.1073/PNAS.85.13.4686
P407
P577
1988-07-01T00:00:00Z