Identification of two independent SUMO-interacting motifs in Daxx: Evolutionary conservation from Drosophila to humans and their biochemical functions

Cell Cycle

Volumn 8, Issue 1, 2009, Pages 76-87

  Santiago, Aleixo ^a   Godsey, Adam C ^a   Hossain, Jamil ^a   Zhao, Lisa Y ^a   Liao, Daiqing ^a,b  

^a UNIVERSITY OF FLORIDA   (United States)

^b UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

Author keywords

c Jun; Molecular evolution; PML body; SUMO interacting motif (SIM); SUMOylation; Transcriptional regulation

Indexed keywords

DAXX PROTEIN; PROTEIN C JUN; PROTEIN UBC9; SUMO PROTEIN; DAXX LIKE PROTEIN, DROSOPHILA; DAXX PROTEIN, HUMAN; DAXX-LIKE PROTEIN, DROSOPHILA; HYDROXAMIC ACID; MUTANT PROTEIN; NUCLEAR PROTEIN; PML PROTEIN, HUMAN; SIGNAL TRANSDUCING ADAPTOR PROTEIN; TRANSCRIPTION FACTOR; TRICHOSTATIN A; TUMOR SUPPRESSOR PROTEIN; UBIQUITIN CONJUGATING ENZYME; UBIQUITIN CONJUGATING ENZYME UBC9; UBIQUITIN-CONJUGATING ENZYME UBC9;

ARTICLE; CELL STRAIN HCT116; CONTROLLED STUDY; DROSOPHILA MELANOGASTER; HUMAN; HUMAN CELL; MOLECULAR EVOLUTION; NONHUMAN; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN MOTIF; PROTEIN PROTEIN INTERACTION; SUMOYLATION; YEAST; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; DRUG EFFECT; GENETIC TRANSCRIPTION; METABOLISM; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PROTEIN BINDING; PROTEIN TERTIARY STRUCTURE; PROTEIN TRANSPORT; SEQUENCE HOMOLOGY;

ANIMALIA; HEXAPODA;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID MOTIFS; AMINO ACID SEQUENCE; ANIMALS; CONSERVED SEQUENCE; DROSOPHILA MELANOGASTER; EVOLUTION, MOLECULAR; HUMANS; HYDROXAMIC ACIDS; MOLECULAR SEQUENCE DATA; MUTANT PROTEINS; NUCLEAR PROTEINS; PROTEIN BINDING; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT; PROTO-ONCOGENE PROTEINS C-JUN; SEQUENCE HOMOLOGY, AMINO ACID; SMALL UBIQUITIN-RELATED MODIFIER PROTEINS; TRANSCRIPTION FACTORS; TRANSCRIPTION, GENETIC; TUMOR SUPPRESSOR PROTEINS; UBIQUITIN-CONJUGATING ENZYMES;

EID: 60749120563     PISSN: 15384101     EISSN: 15514005     Source Type: Journal    
DOI: 10.4161/cc.8.1.7493     Document Type: Article

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