Rad23 interaction with the proteasome is regulated by phosphorylation of its ubiquitin-like (UbL) domain

Journal of Molecular Biology

Volumn 426, Issue 24, 2014, Pages 4049-4060

  Liang, Ruei Yue ^a   Chen, Li ^b   Ko, Bo Ting ^a   Shen, Yu Han ^a   Li, Yen Te ^a   Chen, Bo Rong ^a   Lin, Kuan Ting ^a   Madura, Kiran ^b   Chuang, Show Mei ^a  

^a NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

^b RUTGERS ROBERT WOOD JOHNSON MEDICAL SCHOOL   (United States)

Author keywords

degradation; phosphorylation; proteasome; Rad23; UbL

Indexed keywords

PROTEASOME; PROTEIN; RAD23 PROTEIN; RPN10 PROTEIN; SERINE; THREONINE; UBIQUITIN; UBIQUITINATED PROTEIN; UNCLASSIFIED DRUG; DNA BINDING PROTEIN; DNA LIGASE; PSMD4 PROTEIN, HUMAN; RAD23A PROTEIN, HUMAN; RAD23B PROTEIN, HUMAN; SACCHAROMYCES CEREVISIAE PROTEIN;

ARTICLE; CONTROLLED STUDY; IN VITRO STUDY; IN VIVO STUDY; NONHUMAN; PLEIOTROPY; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN PHOSPHORYLATION; ANIMAL; BINDING SITE; DNA REPAIR; ENZYME SPECIFICITY; GENETICS; HUMAN; IMMUNOBLOTTING; METABOLISM; MOUSE; MUTATION; PHOSPHORYLATION; PROTEIN DEGRADATION; RNA INTERFERENCE; SACCHAROMYCES CEREVISIAE; TUMOR CELL LINE;

ANIMALS; BINDING SITES; CELL LINE, TUMOR; DNA REPAIR; DNA REPAIR ENZYMES; DNA-BINDING PROTEINS; HUMANS; IMMUNOBLOTTING; MICE; MUTATION; PHOSPHORYLATION; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEOLYSIS; RNA INTERFERENCE; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SERINE; SUBSTRATE SPECIFICITY; UBIQUITIN;

EID: 84914680415     PISSN: 00222836     EISSN: 10898638     Source Type: Journal    
DOI: 10.1016/j.jmb.2014.10.004     Document Type: Article

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