Diversity in the architecture of ATLs, a family of plant ubiquitin-ligases, leads to recognition and targeting of substrates in different cellular environments

PLoS ONE

Volumn 6, Issue 8, 2011, Pages

  Aguilar Hernández, Victor ^a   Aguilar Henonin, Laura ^a   Guzmán, Plinio ^a  

^a DEPARTAMENTO DE FÍSICA   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

ATL PROTEIN; PROTEIN DSK2A; RING FINGER PROTEIN; UBIQUILIN; UBIQUITIN PROTEIN LIGASE COP1; UNCLASSIFIED DRUG; VEGETABLE PROTEIN; UBIQUITIN PROTEIN LIGASE;

AMINO TERMINAL SEQUENCE; ARABIDOPSIS; ARTICLE; CONTROLLED STUDY; ENZYME SUBSTRATE; MOLECULAR EVOLUTION; MOLECULAR RECOGNITION; NONHUMAN; PHYLOGENY; PLANT GENE; PLANT GENOME; PROTEIN DOMAIN; PROTEIN FAMILY; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; RICE; SOYBEAN; SPECIES DIFFERENCE; ADAPTATION; CHEMISTRY; GENETICS; METABOLISM; PROTEIN ANALYSIS; RING FINGER MOTIF;

ARABIDOPSIS THALIANA; GLYCINE MAX; ORYZA SATIVA;

ADAPTATION, PHYSIOLOGICAL; GENOME, PLANT; PHYLOGENY; PLANT PROTEINS; PROTEIN INTERACTION DOMAINS AND MOTIFS; PROTEIN INTERACTION MAPPING; RING FINGER DOMAINS; UBIQUITIN-PROTEIN LIGASES;

EID: 84857375684     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0023934     Document Type: Article

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