Serine/threonine kinase 16 and MAL2 regulate constitutive secretion of soluble cargo in hepatic cells

Biochemical Journal

Volumn 463, Issue 2, 2014, Pages 201-213

  In, Julie G ^a,c   Striz, Anneliese C ^a   Bernad, Antonio ^b   Tuma, Pamela L ^a  

^a CATHOLIC UNIVERSITY OF AMERICA   (United States)

^b CENTRO NACIONAL DE INVESTIGACIONES CARDIOVASCULARES CNIC   (Spain)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Albumin; Constitutive secretion; Hepatocyte; Myelin and lymphocyte protein 2 (MAL2); Serine threonine kinase 16 (STK16)

Indexed keywords

ALBUMIN; HAPTOGLOBIN; MUTANT PROTEIN; MYELIN AND LYMPHOCYTE PROTEIN; MYELIN AND LYMPHOCYTE PROTEIN 2; PROTEIN SERINE THREONINE KINASE; PROTEIN SERINE THREONINE KINASE 16; SECRETORY PROTEIN; UBIQUITIN; UNCLASSIFIED DRUG; ALBUMINOID; MAL2 PROTEIN, HUMAN; PROTEIN BINDING; STK16 PROTEIN, HUMAN; TRANSCRIPTION FACTOR;

ACIDIFICATION; ARTICLE; BIOCHEMISTRY; CELL POLARITY; CONTROLLED STUDY; GENE SILENCING; LIVER CELL; LYSOSOME; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROCESSING; PROTEIN PROTEIN INTERACTION; PROTEIN SECRETION; SECRETORY PATHWAY; TEMPERATURE; TRANS GOLGI NETWORK; WILD TYPE; ENZYMOLOGY; GENETICS; HUMAN; METABOLISM; PROTEIN TRANSPORT; TWO HYBRID SYSTEM;

ALBUMINS; HEPATOCYTES; HUMANS; LYSOSOMES; MYELIN AND LYMPHOCYTE-ASSOCIATED PROTEOLIPID PROTEINS; PROTEIN BINDING; PROTEIN TRANSPORT; PROTEIN-SERINE-THREONINE KINASES; TRANS-GOLGI NETWORK; TRANSCRIPTION FACTORS; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 84907205649     PISSN: 02646021     EISSN: 14708728     Source Type: Journal    
DOI: 10.1042/BJ20140468     Document Type: Article

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