Oskar is targeted for degradation by the sequential action of Par-1, GSK-3, and the SCF-Slimb ubiquitin ligase

Developmental Cell

Volumn 26, Issue 3, 2013, Pages 303-314

  Morais de Sá, Eurico ^a,b,c   Vega Rioja, Antonio ^a,b,d   Trovisco, Vítor ^a,b   StJohnston, Daniel ^a,b  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^c UNIVERSITY OF PORTO   (Portugal)

^d HOSPITAL UNIVERSITARIO VIRGEN MACARENA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOGEN SYNTHASE KINASE 3; MESSENGER RNA; OSKAR PROTEIN; PROTEIN; PROTEINASE ACTIVATED RECEPTOR 1; UBIQUITIN PROTEIN LIGASE; UBIQUITIN PROTEIN LIGASE SCF SLIMB; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; MICROTUBULE; NONHUMAN; OOCYTE DEVELOPMENT; POLAR BODY; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN LOCALIZATION; PROTEIN PHOSPHORYLATION; PROTEIN STABILITY; TRANSLATION REGULATION; UBIQUITINATION;

AMINO ACID SEQUENCE; ANIMALS; CELL CYCLE PROTEINS; CELL POLARITY; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; FEMALE; GLYCOGEN SYNTHASE KINASE 3; MOLECULAR SEQUENCE DATA; OOCYTES; OOGENESIS; PHOSPHORYLATION; PROTEIN TRANSPORT; RNA, MESSENGER; SKP CULLIN F-BOX PROTEIN LIGASES; UBIQUITIN-PROTEIN LIGASES; UBIQUITINATION;

EID: 84881486520     PISSN: 15345807     EISSN: 18781551     Source Type: Journal    
DOI: 10.1016/j.devcel.2013.06.011     Document Type: Article

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