Gp78 functions downstream of Hrd1 to promote degradation of misfolded proteins of the endoplasmic reticulum

Molecular Biology of the Cell

Volumn 26, Issue 24, 2015, Pages 4438-4450

  Zhang, Ting ^a   Xu, Yue ^a   Liu, Yanfen ^a,b   Ye, Yihong ^a  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^b SHANGHAITECH UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CHAPERONE; GP78 PROTEIN; HRD1 PROTEIN; PROTEIN; SHORT HAIRPIN RNA; UBIQUITIN PROTEIN LIGASE; UNCLASSIFIED DRUG; AMFR PROTEIN, HUMAN; AUTOCRINE MOTILITY FACTOR RECEPTOR; PROTEIN BINDING; SYVN1 PROTEIN, HUMAN; UBIQUITIN;

ARTICLE; CONTROLLED STUDY; EMBRYO; ENDOPLASMIC RETICULUM; ENDOPLASMIC RETICULUM ASSOCIATED DEGRADATION; ENDOPLASMIC RETICULUM MEMBRANE; GENE SILENCING; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEGRADATION; PROTEIN FOLDING; PROTEIN FUNCTION; SACCHAROMYCES CEREVISIAE; UBIQUITINATION; HEK293 CELL LINE; METABOLISM;

ENDOPLASMIC RETICULUM; ENDOPLASMIC RETICULUM-ASSOCIATED DEGRADATION; HEK293 CELLS; HUMANS; MOLECULAR CHAPERONES; PROTEIN BINDING; PROTEIN FOLDING; PROTEOLYSIS; RECEPTORS, AUTOCRINE MOTILITY FACTOR; UBIQUITIN; UBIQUITIN-PROTEIN LIGASES; UBIQUITINATION;

EID: 84948978497     PISSN: 10591524     EISSN: 19394586     Source Type: Journal    
DOI: 10.1091/mbc.E15-06-0354     Document Type: Article

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