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The RNA Binding G-patch Domain in Retroviral Protease Is important for infectivity and D-type Morphogenesis of Mason-Pfizer Monkey Virus

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22330%2F05%3A00016188" target="_blank" >RIV/60461373:22330/05:00016188 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/05:00028127

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    The RNA Binding G-patch Domain in Retroviral Protease Is important for infectivity and D-type Morphogenesis of Mason-Pfizer Monkey Virus

  • Original language description

    Retroviral proteases (PRs) cleave the viral polyprotein precursorsinto functional mature proteins late during particle release and areessential for viral replication. Unlike most retroviruses, -retroviruses,including Mason-Pfizer monkey virus (M-PMV), assembleimmature capsids within the cytoplasm of the cell. The activation of -retroviral proteases must be highly regulated, because processingof the Gag-related polyprotein precursors occurs only after transportof immature capsids to the plasma membrane and budding.Several -retroviral proteases have unique C-terminal extensionsequences, containing a glycine-rich motif (G-patch), which specificallybinds in vitro to single-stranded nucleic acids. In M-PMV PRthe G-patch is removed in vitro as well as in vivo by autoproteolyticprocessing to yield truncated active forms of PR. To investigate therole of the G-patch domain on the virus life cycle, we introducedmutations within the C-terminal domain of protease.Wefound thatthe G-patch domain of

  • Czech name

    G-patch, RNA vazebná doména v retrovirové protease je důležitá pro infektivitu a morfogenesi D typu Mason-Pfizerova opičího viru

  • Czech description

    Proteasy retrovirů štěpí polyproteinové prekursory na funkční zralé proteiny během uvolňování částic a jsou nezbytné pro replikaci retrovirů. M-PMV skládá nezralé virové částice v cytoplasme. Aktivace proteasy musí být vysoce regulovaný proces, protože štěpení prekursorů se děje pouze po transportu nezralých částic k cytoplasmatické membráně a pučení.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2005

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Biological chemistry

  • ISSN

    0021-9258

  • e-ISSN

  • Volume of the periodical

    280

  • Issue of the periodical within the volume

    51

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    42106-42112

  • UT code for WoS article

  • EID of the result in the Scopus database