Human immunodeficiency virus 1 protease expressed in Escherichia coli behaves as a dimeric aspartic protease.
about
Identification and characterization of a novel retroviral-like aspartic protease specifically expressed in human epidermisP2' Benzene Carboxylic Acid Moiety Is Associated with Decrease in Cellular Uptake: Evaluation of Novel Nonpeptidic HIV-1 Protease Inhibitors Containing P2 bis-Tetrahydrofuran MoietyThioltransferase (glutaredoxin) is detected within HIV-1 and can regulate the activity of glutathionylated HIV-1 protease in vitroIn vitro inhibition of HIV-1 proteinase by ceruleninCopper inhibits the protease from human immunodeficiency virus 1 by both cysteine-dependent and cysteine-independent mechanismsAn inhibitor of the protease blocks maturation of human and simian immunodeficiency viruses and spread of infectionInhibition of human immunodeficiency virus 1 protease in vitro: rational design of substrate analogue inhibitorsAntiretroviral activities of protease inhibitors against murine leukemia virus and simian immunodeficiency virus in tissue cultureMolecular modeling studies suggest that zinc ions inhibit HIV-1 protease by binding at catalytic aspartatesFINDSITE: a threading-based approach to ligand homology modelingConserved cysteines of the human immunodeficiency virus type 1 protease are involved in regulation of polyprotein processing and viral maturation of immature virionsIsolation of mutants of human immunodeficiency virus protease based on the toxicity of the enzyme in Escherichia coli.Stability and activity of human immunodeficiency virus protease: comparison of the natural dimer with a homologous, single-chain tethered dimer.Applications of 3-aminolactams: design, synthesis, and biological evaluation of a library of potential dimerisation inhibitors of HIV1-protease.Strategies for assessing proton linkage to bimolecular interactions by global analysis of isothermal titration calorimetry dataDesign, synthesis and evaluation of a potent substrate analog inhibitor identified by scanning Ala/Phe mutagenesis, mimicking substrate co-evolution, against multidrug-resistant HIV-1 protease.Development of inhibitors of reverse transcriptase and protease as therapeutics against HIV infection.Protocol for rational design of covalently interacting inhibitors.The SIVmac239 Pr55Gag isoform, SIV p43, suppresses proteolytic cleavage of Pr55Gag.Defining the level of human immunodeficiency virus type 1 (HIV-1) protease activity required for HIV-1 particle maturation and infectivitySequence requirements of the HIV-1 protease flap region determined by saturation mutagenesis and kinetic analysis of flap mutantsProteolytic activity of novel human immunodeficiency virus type 1 proteinase proteins from a precursor with a blocking mutation at the N terminus of the PR domain.Human immunodeficiency virus type 1 gag-protease fusion proteins are enzymatically active.Overexpression of the gag-pol precursor from human immunodeficiency virus type 1 proviral genomes results in efficient proteolytic processing in the absence of virion productionHIV-1 protease as a potential target for anti-AIDS therapy.Isolation and characterization of recombinant Drosophila Copia aspartic proteinase.Impact of Stereochemistry on Ligand Binding: X-ray Crystallographic Analysis of an Epoxide-Based HIV Protease Inhibitor.Novel bacteriological assay for detection of potential antiviral agents.Proteolytic processing of Ty3 proteins is required for transposition.Specific inhibitor of human immunodeficiency virus proteinase prevents the cytotoxic effects of a single-chain proteinase dimer and restores particle formation.Identification and characterization of human immunodeficiency virus type 1 gag-pol fusion protein in transfected mammalian cells.Insights into saquinavir resistance in the G48V HIV-1 protease: quantum calculations and molecular dynamic simulations.Cloning and Expression of Soluble Recombinant HIV-1 CRF35 Protease-HP Thioredoxin Fusion Protein.Viral gene products and replication of the human immunodeficiency type 1 virus.Interactions of a novel inhibitor from an extremophilic Bacillus sp. with HIV-1 protease: implications for the mechanism of inactivation.Is the pseudo-dyad in retroviral proteinase monomers structural or evolutionary?Inhibitory effects of Korean medicinal plants and camelliatannin H from Camellia japonica on human immunodeficiency virus type 1 protease.Purification and characterization of human T-cell leukemia virus type I protease produced in Escherichia coli.Competitive inhibition of human immunodeficiency virus type-1 protease by the Gag-Pol transframe protein.Dimerization and activation of the herpes simplex virus type 1 protease.
P2860
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P2860
Human immunodeficiency virus 1 protease expressed in Escherichia coli behaves as a dimeric aspartic protease.
description
1989 nî lūn-bûn
@nan
1989 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի մարտին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@ast
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@en
type
label
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@ast
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@en
prefLabel
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@ast
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@en
P2093
P2860
P356
P1476
Human immunodeficiency virus 1 ...... s a dimeric aspartic protease.
@en
P2093
B D Dayton
B W Metcalf
G B Dreyer
J E Strickler
J G Gorniak
M Rosenberg
V W Magaard
P2860
P304
P356
10.1073/PNAS.86.6.1841
P407
P577
1989-03-01T00:00:00Z