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RNA kink-turns as molecular elbows: Hydration, cation binding, and large-scale dynamics

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F06%3A00015722" target="_blank" >RIV/00216224:14310/06:00015722 - isvavai.cz</a>

  • Alternative codes found

    RIV/68081707:_____/06:00039256

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    RNA kink-turns as molecular elbows: Hydration, cation binding, and large-scale dynamics

  • Original language description

    The presence of Kink-turns (Kt) at key functional sites in the ribosome (e.g., A-site finger and L7/L12 stalk) suggests that some Kink-turns can confer flexibility on RNA protuberances that regulate the traversal of tRNAs during translocation. Explicit solvent molecular dynamics demonstrates that Kink-turns can act as flexible molecular elbows. Kink-turns are associated with a unique network of long-residency static and dynamical hydration sites that is intimately involved in modulating their conformational dynamics. An implicit solvent conformational search confirms the flexibility of Kink-turns around their X-ray geometries and identifies a second low-energy region with open structures that could correspond to Kink-turn geometries seen in solution experiments. An extended simulation of Kt-42 with the factor binding site (helices 43 and 44) shows that the local Kt-42 elbow-like motion fully propagates beyond the Kink-turn, and that there is no other comparably flexible site in this rR

  • Czech name

    RNA kink-turn jako molekulové lokty: Hydratace, vazba iontů a dynamika

  • Czech description

    K-turn motivy jsou funkční klíčové RNA elementy (např:A-site finger and L7/L12 stalk), které regulují flexibilitu ribosomální RNA během procesu translokace. Explicit solvent MD simulace ukazují, že tyto struktury jsou asociovány se sití molekul vod, které významně ovlivňují jejich konformace.

Classification

  • Type

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

  • CEP classification

    CF - Physical chemistry and theoretical chemistry

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2006

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Structure

  • ISSN

    0969-2126

  • e-ISSN

  • Volume of the periodical

    14

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    825-835

  • UT code for WoS article

  • EID of the result in the Scopus database