RN-tre specifically binds to the SH3 domain of eps8 with high affinity and confers growth advantage to NIH3T3 upon carboxy-terminal truncation

Oncogene

Volumn 12, Issue 12, 1996, Pages 2679-2688

  Matòšková, Broňa ^a,b   Wong, William T ^c   Nomura, Nobuo ^d   Robbins, Keith C ^b   Di Fiore, Pier Paolo ^a,e  

^a EUROPEAN INSTITUTE OF ONCOLOGY   (Italy)

^b NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

^d KAZUSA DNA RESEARCH INSTITUTE   (Japan)

^e UNIVERSITY OF BARI MEDICAL SCHOOL   (Italy)

Author keywords

eps8; SH3; Signal transduction; tre

Indexed keywords

COMPLEMENTARY DNA; MUTANT PROTEIN; ONCOPROTEIN; PROTEIN; PROTEIN TYROSINE KINASE; SH3 DOMAIN PROTEIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; CARBOXY TERMINAL SEQUENCE; CELL PROLIFERATION; CELL STRAIN 3T3; CONTROLLED STUDY; GENE ISOLATION; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN PROTEIN INTERACTION; STRUCTURE ACTIVITY RELATION;

3T3 CELLS; ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ANIMALS; CELL DIVISION; CYTOSKELETAL PROTEINS; GENETIC VECTORS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MICE; ONCOGENE PROTEINS, FUSION; PROTEINS; RECOMBINANT PROTEINS; SRC HOMOLOGY DOMAINS; SUBSTRATE SPECIFICITY;

ANIMALIA;

EID: 0029884459     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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