Chin C C, Brewer J M, Wold F
J Biol Chem. 1981 Feb 10;256(3):1377-84.
Automatic sequencing of yeast enolase and of its chemically and enzymatically produced peptide fragments has established the sequence of 416 of the 436 residues in the enolase subunits. The missing segments have been provided from results from sequencing the DNA of the yeast enolase genes (Holland, M. J., Holland, J. P., Thill, G. P., and Jackson, K. A. (1981) J. Biol. Chem. 256, 1385-1395). The reported enolase sequence thus represents the results of two completely independent studies, which yielded identical results for 404 of the 436 residues, and which on re-examination are consistent with the reported sequence in all but nine positions. The availability of the entire yeast enolase sequence has permitted a reassessment of structure-function parameters available for the enzyme, and some implications of the sequence information on the secondary, tertiary, and quarternary structure and on the active site components of yeast enolase have been summarized and discussed.
对酵母烯醇化酶及其化学和酶促产生的肽片段进行自动测序,已确定烯醇化酶亚基436个残基中的416个残基的序列。缺失的片段已根据酵母烯醇化酶基因DNA测序结果补齐(霍兰德,M. J.,霍兰德,J. P.,蒂尔,G. P.,以及杰克逊,K. A.(1981年)《生物化学杂志》256,1385 - 1395)。因此,所报道的烯醇化酶序列代表了两项完全独立研究的结果,这两项研究对436个残基中的404个残基得出了相同的结果,并且在重新检查时,除了九个位置外,其余都与所报道的序列一致。完整的酵母烯醇化酶序列的可得性使得能够重新评估该酶的结构 - 功能参数,并且总结并讨论了序列信息对酵母烯醇化酶的二级、三级和四级结构以及活性位点组成的一些影响。