Bayney R M, Rodkey J A, Bennett C D, Lu A Y, Pickett C B
J Biol Chem. 1987 Jan 15;262(2):572-5.
We have determined the nucleotide sequence of a cDNA clone, pDTD55, complementary to rat liver quinone reductase mRNA (Williams, J.B., Lu, A.Y.H., Cameron, R.G., and Pickett, C.B. (1986) J. Biol. Chem. 261, 5524-5528). The cDNA clone contains an open reading frame of 759 nucleotides encoding a polypeptide comprised of 253 amino acids with a Mr = 28,564. To verify the predicted amino acid sequence of quinone reductase, we have been able to align the amino acid sequences of a cyanogen bromide digest of the purified enzyme to the sequence deduced from the cDNA clone. A comparison of the quinone reductase sequence with other known flavoenzymes did not reveal a significant degree of amino acid sequence homology. These data suggest that the quinone reductase gene has evolved independently from genes encoding other flavoenzymes.
我们已经确定了一个与大鼠肝脏醌还原酶mRNA互补的cDNA克隆pDTD55的核苷酸序列(Williams, J.B., Lu, A.Y.H., Cameron, R.G., 和Pickett, C.B. (1986) J. Biol. Chem. 261, 5524 - 5528)。该cDNA克隆包含一个759个核苷酸的开放阅读框,编码一个由253个氨基酸组成的多肽,其Mr = 28,564。为了验证醌还原酶预测的氨基酸序列,我们已能够将纯化酶的溴化氰消化产物的氨基酸序列与从cDNA克隆推导的序列进行比对。醌还原酶序列与其他已知黄素酶的比较未显示出显著程度的氨基酸序列同源性。这些数据表明醌还原酶基因已从编码其他黄素酶的基因中独立进化而来。