Specific amino acid residues in the basic helix-loop-helix domain of SRC-3 are essential for its nuclear localization and proteasome-dependent turnover

Molecular and Cellular Biology

Volumn 27, Issue 4, 2007, Pages 1296-1308

  Li, Chao ^a   Wu, Ray Chang ^a   Amazit, Larbi ^a   Tsai, Sophia Y ^a   Tsai, Ming Jer ^a   O'Malley, Bert W ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXIMIDE; ESTROGEN RECEPTOR; HELIX LOOP HELIX PROTEIN; PROTEASOME; STEROID RECEPTOR COACTIVATOR 3; VIRUS ANTIGEN;

AMINO ACID ANALYSIS; ANIMAL CELL; ARTICLE; CANCER GROWTH; CELL GROWTH; CELLULAR DISTRIBUTION; CYTOPLASM; GENE MUTATION; HUMAN; HUMAN CELL; NONHUMAN; NUCLEAR LOCALIZATION SIGNAL; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN LOCALIZATION; PROTEIN STABILITY; SIMIAN VIRUS 40; TIME; TRANSCRIPTION REGULATION;

ACTIVE TRANSPORT, CELL NUCLEUS; AMINO ACID SEQUENCE; ANTIGENS, POLYOMAVIRUS TRANSFORMING; ARGININE; CELL GROWTH PROCESSES; CELL NUCLEUS; CYTOPLASM; GENES, REPORTER; HELA CELLS; HELIX-LOOP-HELIX MOTIFS; HISTONE ACETYLTRANSFERASES; HUMANS; LYSINE; MOLECULAR SEQUENCE DATA; MUTANT PROTEINS; NUCLEAR LOCALIZATION SIGNALS; PROTEASOME ENDOPEPTIDASE COMPLEX; PROTEIN STRUCTURE, TERTIARY; STRUCTURE-ACTIVITY RELATIONSHIP; THERMODYNAMICS; TRANS-ACTIVATORS; TRANSCRIPTION, GENETIC;

SIMIAN VIRUS 40;

EID: 33846928412     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.00336-06     Document Type: Article

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