Origin and evolution of the cystic fibrosis transmembrane regulator protein R domain

Gene

Volumn 523, Issue 2, 2013, Pages 137-146

  Sebastian, Aswathy ^a   Rishishwar, Lavanya ^a   Wang, Jianrong ^a   Bernard, Karen F ^b   Conley, Andrew B ^a   McCarty, Nael A ^b   Jordan, I King ^a,c  

^a GEORGIA INSTITUTE OF TECHNOLOGY   (United States)

^b CHILDREN'S HEALTHCARE OF ATLANTA   (United States)

^c PanAmerican Bioinformatics Institute   (Colombia)

Author keywords

Coding sequence; Cystic fibrosis; Molecular evolution; Neo functionalization; R domain

Indexed keywords

ABC TRANSPORTER; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR;

ARTICLE; EVOLUTIONARY RATE; EXON; GENE CONTROL; GENE FUNCTION; GENE INTERACTION; GENE SEQUENCE; GENE STRUCTURE; GENETIC SELECTION; HUMAN; INTRON; MOLECULAR EVOLUTION; PHYLOGENY; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN PHOSPHORYLATION; RNA SPLICING; SEQUENCE HOMOLOGY; AMINO ACID SEQUENCE; ANIMAL; CELL LINEAGE; CHEMISTRY; GENE ORDER; GENETICS; MOLECULAR GENETICS; POSITION WEIGHT MATRIX;

AMINO ACID SEQUENCE; ANIMALS; ATP-BINDING CASSETTE TRANSPORTERS; CELL LINEAGE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; EVOLUTION, MOLECULAR; EXONS; GENE ORDER; HUMANS; MOLECULAR SEQUENCE DATA; PHYLOGENY; POSITION-SPECIFIC SCORING MATRICES; PROTEIN INTERACTION DOMAINS AND MOTIFS; RNA SPLICE SITES;

MLCS; MLOWN;

EID: 84880428551     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2013.02.050     Document Type: Article

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