The E3 ubiquitin ligase parkin is recruited to the 26 S proteasome via the proteasomal ubiquitin receptor Rpn13

Journal of Biological Chemistry

Volumn 290, Issue 12, 2015, Pages 7492-7505

  Aguileta, Miguel A ^a   Korac, Jelena ^b   Durcan, Thomas M ^a   Trempe, Jean Franҫois ^c   Haber, Michael ^a   Gehring, Kalle ^c   Elsasser, Suzanne ^d   Waidmann, Oliver ^e   Fon, Edward A ^a   Husnjak, Koraljka ^e  

^a MCGILL UNIVERSITY   (Canada)

^b UNIVERSITY OF SPLIT   (Croatia)

^c MCGILL UNIVERSITY   (Canada)

^d HARVARD MEDICAL SCHOOL   (United States)

^e GOETHE UNIVERSITY MEDICAL SCHOOL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE ENCODING; MITOCHONDRIA;

AUTOUBIQUITINATION; CELLULAR PROCESS; HYDROPHOBIC PATCH; MITOCHONDRIAL PROTEIN; MUTATIONAL ANALYSIS; PARKINSON DISEASE; TARGET PROTEINS; UBIQUITIN LIGASES;

PROTEINS;

MEMBRANE PROTEIN; MITOCHONDRIAL PROTEIN; PARKIN; PROTEASOME; PROTEIN RPN13; PROTEIN TIM23; PROTEIN TIM44; TRANSLOCASE OF OUTER MITOCHONDRIAL MEMBRANE 20; UBIQUITIN; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG; ADRM1 PROTEIN, HUMAN; ATP DEPENDENT 26S PROTEASE; UBIQUITIN PROTEIN LIGASE;

AMINO TERMINAL SEQUENCE; ARTICLE; BINDING AFFINITY; CHROMATIN IMMUNOPRECIPITATION; CONTROLLED STUDY; HUMAN; HUMAN CELL; HYDROPHOBICITY; MEMBRANE DEPOLARIZATION; MITOPHAGY; MUTATIONAL ANALYSIS; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PLASMID; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN METABOLISM; PROTEIN PHOSPHORYLATION; PROTEIN PROTEIN INTERACTION; PROTEIN PURIFICATION; SACCHAROMYCES CEREVISIAE; SURFACE PLASMON RESONANCE; GENETICS; HEK293 CELL LINE; METABOLISM; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NUCLEOTIDE SEQUENCE; TWO HYBRID SYSTEM;

BASE SEQUENCE; HEK293 CELLS; HUMANS; MAGNETIC RESONANCE SPECTROSCOPY; MEMBRANE GLYCOPROTEINS; PROTEASOME ENDOPEPTIDASE COMPLEX; SURFACE PLASMON RESONANCE; TWO-HYBRID SYSTEM TECHNIQUES; UBIQUITIN-PROTEIN LIGASES;

EID: 84925340816     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M114.614925     Document Type: Article

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