Wach A, Schlesser A, Goffeau A
Unité de Biochimie Physiologique, Université Catholique de Louvain, Belgium.
J Bioenerg Biomembr. 1992 Jun;24(3):309-17. doi: 10.1007/BF00768851.
Seventeen protein sequences of H(+)-ATPases from plants (Arabidopsis thaliana, Nicotiana plumbaginifolia, Lycopersicum esculentum), fungi (Saccharomyces cerevisiae, Schizosaccharomyces pombe, Zygosaccharomyces rouxii, Neuropora crassa, Candida albicans), and a parasitic ciliate (Leishmania donovani) have been aligned. Twenty sequence fragments were identified which were conserved in H(+)-, Na+/K(+)-, and Ca++ plasma membrane-ATPases. In addition, a total of 118 residues not located in these fragments were found to be conserved in all H(+)-ATPases. Among those, 38 amino acid residues were screened out as being priority targets for site-directed mutagenesis experiments aimed at the identification of the amino acid residues specifically involved in cation specificity.
已对来自植物(拟南芥、烟草、番茄)、真菌(酿酒酵母、粟酒裂殖酵母、鲁氏酵母、粗糙脉孢菌、白色念珠菌)和一种寄生纤毛虫(杜氏利什曼原虫)的17种H(+)-ATP酶的蛋白质序列进行了比对。鉴定出20个在H(+)-、Na+/K(+)-和Ca++质膜ATP酶中保守的序列片段。此外,发现在所有H(+)-ATP酶中共有118个不在这些片段中的残基是保守的。其中,筛选出38个氨基酸残基作为定点诱变实验的优先靶点,旨在鉴定与阳离子特异性专门相关的氨基酸残基。