Nishimura C, Tamura T, Tokunaga F, Tanaka K, Ichihara A
Laboratory of Applied Toxicology, Nippon Kayaku Co. Ltd., Gunma, Japan.
FEBS Lett. 1993 Oct 11;332(1-2):52-6. doi: 10.1016/0014-5793(93)80482-a.
The nucleotide sequence of a cDNA that encodes a new subunit, named RC7-I, of the 20 S proteasome of rat hepatoma cells has been determined. The polypeptide predicted from the open reading frame consists of 201 amino acid residues with a calculated molecular weight of 22,912 and isoelectric point of 7.25. Approximately 80% of the partial amino acid sequences of several fragments of RC7-I, determined by protein chemical analyses, were found to be in excellent accordance with those deduced from the cDNA sequence. Computer analysis showed that RC7-I belongs to the beta-type subgroup of proteasomes with similarity to the beta-subunit of the archaebacterial proteasome, differing clearing from alpha-type subunits of the proteasome gene family. The overall structure of RC7-I was found to be homologous to that of yeast PRE1, which is necessary for chymotryptic activity.
已确定编码大鼠肝癌细胞20S蛋白酶体新亚基(命名为RC7-I)的cDNA的核苷酸序列。从开放阅读框预测的多肽由201个氨基酸残基组成,计算分子量为22912,等电点为7.25。通过蛋白质化学分析确定的RC7-I几个片段的部分氨基酸序列中,约80%与从cDNA序列推导的序列高度一致。计算机分析表明,RC7-I属于蛋白酶体的β型亚组,与古细菌蛋白酶体的β亚基相似,与蛋白酶体基因家族的α型亚基明显不同。发现RC7-I的整体结构与酵母PRE1同源,PRE1是胰凝乳蛋白酶活性所必需的。