Unraveling the function of Arabidopsis thaliana OS9 in the endoplasmic reticulum-associated degradation of glycoproteins

Plant Molecular Biology

Volumn 79, Issue 1-2, 2012, Pages 21-33

  Hüttner, Silvia ^a   Veit, Christiane ^a   Schoberer, Jennifer ^a,b   Grass, Josephine ^a   Strasser, Richard ^a  

^a UNIVERSITY OF NATURAL RESOURCES AND LIFE SCIENCES   (Austria)

^b OXFORD BROOKES UNIVERSITY   (United Kingdom)

Author keywords

ER stress; ERAD; Posttranslational modification; Protein glycosylation; Protein quality control; Unfolded protein response

Indexed keywords

ARABIDOPSIS PROTEIN; GLYCOPROTEIN; GREEN FLUORESCENT PROTEIN; HYBRID PROTEIN; MEMBRANE PROTEIN; OS9 PROTEIN, ARABIDOPSIS; POLYSACCHARIDE; SODIUM CHLORIDE;

AMINO ACID SEQUENCE; ARABIDOPSIS; ARTICLE; CHEMISTRY; DRUG EFFECT; ENDOPLASMIC RETICULUM; ENDOPLASMIC RETICULUM ASSOCIATED DEGRADATION; GENETICS; METABOLISM; MOLECULAR GENETICS; MUTATION; PHENOTYPE; PHYSIOLOGICAL STRESS; PROTEIN BINDING; PROTEIN TERTIARY STRUCTURE; SACCHAROMYCES CEREVISIAE; UNFOLDED PROTEIN RESPONSE;

AMINO ACID SEQUENCE; ARABIDOPSIS; ARABIDOPSIS PROTEINS; ENDOPLASMIC RETICULUM; ENDOPLASMIC RETICULUM-ASSOCIATED DEGRADATION; GLYCOPROTEINS; GREEN FLUORESCENT PROTEINS; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; POLYSACCHARIDES; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; RECOMBINANT FUSION PROTEINS; SACCHAROMYCES CEREVISIAE; SODIUM CHLORIDE; STRESS, PHYSIOLOGICAL; UNFOLDED PROTEIN RESPONSE;

ARABIDOPSIS; ARABIDOPSIS THALIANA; MAMMALIA;

EID: 84860015488     PISSN: 01674412     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11103-012-9891-4     Document Type: Article

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