Modular structure of glucocorticoid receptor domains not equivalent to functional independence. Stability and activity of the steroid binding domain are controlled by sequences in separate domains

Journal of Biological Chemistry

Volumn 271, Issue 35, 1996, Pages 21430-21438

  Xu, Min ^a   Chakraborti, Pradip K ^a,c   Garabedian, Michael J ^b,d   Yamamoto, Keith R ^b   Simons Jr , S Stoney ^a  

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

^b UNIVERSITY OF CALIFORNIA   (United States)

^c INSTITUTE OF MICROBIAL TECHNOLOGY   (India)

^d NEW YORK UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GALACTOSIDASE; DIHYDROFOLATE REDUCTASE; GLUCOCORTICOID; HYBRID PROTEIN; MUTANT PROTEIN; STEROID HORMONE;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CELL STRAIN COS1; CONTROLLED STUDY; HORMONE RECEPTOR INTERACTION; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN FOLDING; PROTEIN STABILITY; THERMOSTABILITY;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; DEXAMETHASONE; DNA PRIMERS; HYDROLYSIS; MOLECULAR SEQUENCE DATA; PLASMIDS; PROTEIN CONFORMATION; RATS; RECEPTORS, GLUCOCORTICOID; TRYPSIN;

ANIMALIA;

EID: 0029829893     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.271.35.21430     Document Type: Article

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