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Sheep 6-phosphogluconate dehydrogenase. Revised protein sequence based upon the sequences of cDNA clones obtained with the polymerase chain reaction

机译:绵羊6-磷酸葡萄糖酸脱氢酶。根据通过聚合酶链反应获得的cDNA克隆序列修改的蛋白质序列

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pSheep liver 6-phosphogluconate dehydrogenase (6-PGDH) is an enzyme of the pentose phosphate pathway. Evidence has appeared which suggests that the 6-PGDH protein sequence determined previously by direct analysis of the protein isolated from ovine liver is incorrect. Determining the enzyme9s DNA sequence was considered to be the best way of solving the problem. In the first instance, a degenerate forward and a degenerate reverse primer were designed on the basis of the known protein sequence, and a partial-length cDNA clone was isolated from total sheep liver cDNA using the polymerase chain reaction. The clone encoded the expected part of the protein sequence. The clone was unsuccessfully used as a prime-cut probe to screen a sheep liver library and a bovine heart library. As a result, the polymerase chain reaction was utilized again to successfully generate a family of overlapping cDNA clones encoding a mature protein of 482 amino acids. The mature protein sequence encoded by the cDNA differs significantly from the sequence derived by direct analysis of the protein, but on closer examination the fundamental difference is caused by the incorrect placement of three enzyme fragments obtained by cyanogen bromide cleavage during the direct sequence analysis of the protein. Placing the fragments in the correct order results in the two sequences being virtually identical except for some minor amino acid changes between the amide and acid forms, and a small number of deletions and insertions./p
机译:绵羊肝6-磷酸葡萄糖酸酯脱氢酶(6-PGDH)是戊糖磷酸途径的酶。已有证据表明,先前通过直接分析从羊肝分离的蛋白质而直接确定的6-PGDH蛋白质序列是不正确的。确定酶的DNA序列被认为是解决该问题的最佳方法。首先,根据已知的蛋白质序列设计简并正向和简并反向引物,并使用聚合酶链反应从羊肝总cDNA中分离出部分长度的cDNA克隆。该克隆编码蛋白质序列的预期部分。该克隆未能成功用作筛选绵羊肝文库和牛心脏文库的主要探针。结果,再次利用聚合酶链反应成功地产生了一个重叠的cDNA克隆家族,该克隆编码了482个氨基酸的成熟蛋白。由cDNA编码的成熟蛋白质序列与直接分析该蛋白质所衍生的序列有显着差异,但是在仔细检查中,根本差异是由于在直接测序分析过程中溴化氰裂解得到的三个酶片段的错误放置所引起的。蛋白。以正确的顺序放置片段会导致两个序列几乎相同,除了酰胺和酸形式之间的一些小氨基酸变化以及少量的缺失和插入。

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