Kopetzki E, Entian K D, Mecke D
Gene. 1985;39(1):95-101. doi: 10.1016/0378-1119(85)90113-1.
The nucleotide sequence of the yeast glycolytic hexokinase isoenzyme PI-gene, HXK1, has been determined by sequencing the yeast DNA insert of the previously isolated plasmid HXK1 clone [Entian et al., Mol. Gen. Genet. 198 (1984) 50-54]. The structural gene sequence included 1452 bp coding for 484 amino acid (aa) residues corresponding to the Mr of 153 605 for the HXK1 monomer. Several initiation regions and termination points were located using nuclease S1 mapping. The HXK1 sequence was 76% homologous with that of HXK2, which is responsible for triggering glucose repression in yeasts. Since HXK1 is not involved in this regulatory system, the regulatory function of HXK2 must correspond to one or more of the differences between both isoenzymes. Most changes in the amino acid sequence were statistically distributed; however, four clustered regions with more than five altered aa residues were identified.
已通过对先前分离的质粒HXK1克隆的酵母DNA插入片段进行测序,确定了酵母糖酵解己糖激酶同工酶PI基因HXK1的核苷酸序列[恩田等人,《分子与普通遗传学》198(1984)50 - 54]。结构基因序列包含1452个碱基对,编码484个氨基酸残基,对应HXK1单体的相对分子质量为153605。使用核酸酶S1图谱定位了几个起始区域和终止点。HXK1序列与HXK2的序列同源性为76%,HXK2负责引发酵母中的葡萄糖阻遏。由于HXK1不参与该调节系统,HXK2的调节功能必定对应于这两种同工酶之间的一个或多个差异。氨基酸序列中的大多数变化呈统计学分布;然而,鉴定出了四个聚集区域,其中有超过五个氨基酸残基发生了改变。