Lusty C J, Widgren E E, Broglie K E, Nyunoya H
J Biol Chem. 1983 Dec 10;258(23):14466-77.
A cloned fragment of yeast chromosomal DNA carrying the gene CPA2 coding for the large subunit of arginine-specific carbamyl phosphate synthetase has been sequenced. The cloned DNA has a 3,354-nucleotide long continuous reading frame coding for a polypeptide of 1,117 amino acids. The calculated molecular weight of the encoded polypeptide is 123,787, in good agreement with the reported molecular weight of the yeast carbamyl phosphate synthetase large subunit. The amino acid sequence of yeast carbamyl phosphate synthetase is homologous to the recently determined sequence of Escherichia coli carbamyl phosphate synthetase (Nyunoya, H., and Lusty, C. J. (1983) Proc. Natl. Acad. Sci. U. S. A. 80, 4629-4633) over almost the entire length of the protein. Like the E. coli large subunit, the yeast enzyme exhibits an extensive internal homology between its NH2- and carboxyl-terminal halves. The internal homology in both the yeast and E. coli proteins indicates that the gene coding for the large subunit of carbamyl phosphate synthetase was derived from a tandem duplication which occurred prior to the divergence of eukaryotes and prokaryotes.
一个携带编码精氨酸特异性氨甲酰磷酸合成酶大亚基的基因CPA2的酵母染色体DNA克隆片段已被测序。该克隆DNA有一个3354个核苷酸长的连续阅读框,编码一个由1117个氨基酸组成的多肽。所编码多肽的计算分子量为123787,与报道的酵母氨甲酰磷酸合成酶大亚基的分子量非常一致。酵母氨甲酰磷酸合成酶的氨基酸序列在几乎整个蛋白质长度上与最近确定的大肠杆菌氨甲酰磷酸合成酶序列(Nyunoya, H., and Lusty, C. J. (1983) Proc. Natl. Acad. Sci. U. S. A. 80, 4629 - 4633)同源。与大肠杆菌大亚基一样,酵母酶在其氨基末端和羧基末端两半之间表现出广泛的内部同源性。酵母和大肠杆菌蛋白质中的内部同源性表明,编码氨甲酰磷酸合成酶大亚基的基因源自真核生物和原核生物分化之前发生的串联重复。