Počet záznamů: 1  

Phenyl- and benzylurea cytokinins as competitive inhibitors of cytokinin oxidase/dehydrogenase: a structural study

  1. 1.
    SYSNO ASEP0359309
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevPhenyl- and benzylurea cytokinins as competitive inhibitors of cytokinin oxidase/dehydrogenase: a structural study
    Tvůrce(i) Kopečný, D. (CZ)
    Briozzo, P. (FR)
    Popelková, H. (US)
    Šebela, M. (CZ)
    Končitíková, R. (CZ)
    Spíchal, Lukáš (UEB-Q) RID, ORCID
    Nisler, Jaroslav (UEB-Q) RID, ORCID
    Madzak, C. (FR)
    Frébort, Ivo (UEB-Q)
    Laloue, M. (FR)
    Houba-Herin, N. (FR)
    Celkový počet autorů11
    Zdroj.dok.Biochimie. - : Elsevier - ISSN 0300-9084
    Roč. 92, č. 8 (2010), s. 1052-1062
    Poč.str.11 s.
    Jazyk dok.eng - angličtina
    Země vyd.FR - Francie
    Klíč. slovabenzylurea ; crystal structure ; cytokinin oxidase/dehydrogenase
    Vědní obor RIVCE - Biochemie
    CEPGA522/08/0555 GA ČR - Grantová agentura ČR
    GA301/08/1649 GA ČR - Grantová agentura ČR
    CEZAV0Z50380511 - UEB-Q (2005-2011)
    UT WOS000280570800018
    DOI10.1016/j.biochi.2010.05.006
    AnotaceCytokinin oxidase/dehydrogenase (CKO) is a flavoenzyme, which irreversibly degrades the plant hormones cytokinins. An inhibitory study with numerous urea derivatives was undertaken using the maize enzyme (ZmCKO1) and the crystal structure of ZmCKO1 in a complex with N-(2-chloro-pyridin-4-yl)-N´-phenylurea (CPPU) was solved. Subsequently, site-directed mutagenesis of L492 and E381 residues involved in the inhibitor binding was performed. The crystal structures of L492A mutant in a complex with CPPU and N-(2-chloro-pyridin-4-yl)-N´-benzylurea (CPBU) were solved and confirm the importance of a stacking interaction between the 2-chloro-4-pyridinyl ring of the inhibitor and the isoalloxazine ring of the FAD cofactor. As highly specific CKO inhibitors without undesired side effects are of major interest for physiological studies, all studied compounds were further analyzed for cytokinin activity in the Amaranthus bioassay and for binding to the Arabidopsis cytokinin receptors AHK3 and AHK4.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2012
Počet záznamů: 1  

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