Drosophila protein kinase CK2 is rendered temperature-sensitive by mutations of highly conserved residues flanking the activation segment

Molecular and Cellular Biochemistry

Volumn 323, Issue 1-2, 2009, Pages 49-60

  Kuntamalla, Pallavi P ^a   Kunttas Tatli, Ezgi ^a   Karandikar, Umesh ^a   Bishop, Clifton P ^a   Bidwai, Ashok P ^a  

^a WEST VIRGINIA UNIVERSITY   (United States)

Author keywords

CK2; Drosophila; Protein kinase; Temperature sensitive

Indexed keywords

ASPARAGINE; ASPARTIC ACID; CASEIN KINASE II; SERINE; THREONINE;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CONTROLLED STUDY; CRYSTAL STRUCTURE; DROSOPHILA; GENETIC CONSERVATION; MUTATIONAL ANALYSIS; NONHUMAN; PROTEIN INTERACTION; PROTEIN STABILITY; TEMPERATURE SENSITIVITY;

AMINO ACID SEQUENCE; ANIMALS; CASEIN KINASE II; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; ENZYME ACTIVATION; HUMANS; MICE; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN CONFORMATION; SEQUENCE ALIGNMENT; TEMPERATURE;

ANIMALIA;

EID: 59949105892     PISSN: 03008177     EISSN: 15734919     Source Type: Journal    
DOI: 10.1007/s11010-008-9963-6     Document Type: Article

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