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J. Biol. Chem., Vol. 259, Issue 24, 15224-15227, Dec, 1984
CP Ordahl, GL Evans, TA Cooper, G Kunz and JC Perriard
cDNA clones of chick muscle creatine kinase mRNA were prepared by
conventional procedures and then extended by primer extension to include
the entire coding region of the mRNA. The nucleotide sequence of the cDNA
clones permits, for the first time, determination of the complete sequence
of the 381 amino acids comprising the muscle creatine kinase subunit of a
higher vertebrate. In addition, available information regarding amino acid
residues, intergral or proximal to the active site, allows tentative
positioning of part of the active site within the primary sequence.
Comparison of the chick muscle creatine kinase amino acid sequence with
partial amino acid sequence for rat and rabbit muscle creatine kinase
indicates that the primary structure of this enzyme is strongly conserved
in evolution.
Complete cDNA-derived amino acid sequence of chick muscle creatine kinase
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