Benfield P A, Zivin R A, Miller L S, Sowder R, Smythers G W, Henderson L, Oroszlan S, Pearson M L
J Biol Chem. 1984 Dec 10;259(23):14979-84.
A series of cDNA clones corresponding to 1494 bases of rat muscle creatine kinase mRNA has been isolated and characterized. The identity of these clones has been confirmed by DNA sequence analysis and by comparison of the predicted amino acid sequence with that determined for the purified protein. The cDNA sequence accounts for the entire coding sequence of the creatine kinase protein in addition to the complete 3' untranslated region and 68 bases of 5' noncoding region. Sequences corresponding to the active site region of the protein, the initiation codon, the termination codon, and poly(A) addition signal have been identified.
一系列与大鼠肌肉肌酸激酶mRNA的1494个碱基相对应的cDNA克隆已被分离和鉴定。这些克隆的身份已通过DNA序列分析以及将预测的氨基酸序列与纯化蛋白的氨基酸序列进行比较得以证实。该cDNA序列除了完整的3'非翻译区和5'非编码区的68个碱基外,还包含肌酸激酶蛋白的整个编码序列。已鉴定出与该蛋白活性位点区域、起始密码子、终止密码子和聚腺苷酸添加信号相对应的序列。