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Titlebook: Retroviral Proteases; Control of maturatio Laurence H. Pearl Textbook 1990Latest edition Macmillan Publishers Limited 1990 AIDS.biology.evo

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Hans R. Gelderblom,Preston A. Marx,Muhsin Özel,Dirk Gheysen,Robert J. Munn,Kenneth I. Joy,Georg Paulal mediazation impact on processes of negotiating contempora.This innovative volume explores the link between local and regional eating cultures and their mediatization via transnational TV cooking shows, glocal food advertising and social media transfer of recipes. Pursuing a global and interdiscip
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is. In Maastricht (the Netherlands) the monetary union was agreed. The negotiations for the Maastricht Treaty took place during upheaval in Central and Eastern Europe when the divide between Eastern and Western Europe was suddenly lifted, and the EU was faced with the historic challenge of uniting E
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Retroviral Protease: Substrate Specificity and Inhibitors, genomes encode proteinases. The enzymes work as a processing enzyme which cleaves viral polyprotein precursors into mature components. The precursor processing is essential for production of biologically active virus particles (Klausslich and Wimmer, 1988).
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Morphogenesis of Retroviruses: A Complex Role for the Matrix (MA) Protein in Assembly, Stability anprotein core composed of genomic RNA and structural protein subunits (Nermut ., 1972; Marx ., 1988). The morphology of the core is somewhat virus specific and may be spherical (Rous sarcoma virus, RSV), rod-shaped (Mason-Pfizer monkey virus, M-PMV) or cone-shaped (human immunodeficiency virus, HIV) in electron micrographs.
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Morphogenesis, Maturation and Fine Structure of Lentiviruses,ed proteins (Desrosiers ., 1989). Serological cross-reactivities localized mainly to the viral core, but also to the envelope, have been described for HIV and EIAV (Montagnier ., 1984; Montelaro ., 1988; Schneider ., 1986, 1987).
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The HIV-1 Aspartyl Protease: Maturation and Substrate Specificity, case of HIV-1 (Rey ., 1987; Jacks ., 1988). Experimental evidence strongly suggests that HIV-1 viral particles initially bud out of the host cell with an immature structure and composition, containing unprocessed PrSSgag and Pr160gag-Pol polyproteins (Hockley . ., 1988; Gottlinger ., 1989, Peng .,
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Cleavage of RT/RNase H by HIV-1 Protease and Analysis of Substrate Cleavage Sites ,, the p32 endonuclease and the p9 protease. The partially purified protease generates . from the p66 molecule a p66/p51 heterodimer, typical of the normally observed RT/RNase H, and a p15 carboxyterminal fragment. A synthetic peptide AETF’YVD derived from the p51/p15 junction is cleaved by the prote
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Retroviral Protease: Substrate Specificity and Inhibitors,nthesized as polyprotein precursors and assembled to form immature particles. Those precursors are processed into functional components by proteinases. This type of assembly may be more accurate and economical than a system where particles are formed by assembling separate proteins with distinct pro
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