Nelissen B, De Wachter R, Goffeau A
Departement Biochemie, Universiteit Antwerpen (UIA), Belgium.
FEMS Microbiol Rev. 1997 Sep;21(2):113-34. doi: 10.1111/j.1574-6976.1997.tb00347.x.
On the basis of the complete genome sequence of the budding yeast Saccharomyces cerevisiae, a computer-aided analysis was carried out of all members of the major facilitator superfamily (MFS), which typically consists of permeases with 12 transmembrane spans. Analysis of all 5885 predicted open reading frames identified 186 potential MFS proteins. Binary sequence comparison made it possible to cluster 149 of them into 23 families. Putative permease functions could be assigned to 12 families, the largest including sugar, amino acid, and multidrug transport. Phylogenetic clustering of proteins allowed us to predict a possible permease function for a total of 119 proteins. Multiple sequence alignments were made for all families, and evolutionary trees were constructed for families with at least four members. The latter resulted in the identification of 21 subclusters with presumably tightly related permease function. No functional clues were predicted for a total of 41 clustered or unclustered proteins.
基于芽殖酵母酿酒酵母的全基因组序列,对主要转运体超家族(MFS)的所有成员进行了计算机辅助分析,该超家族通常由具有12个跨膜结构域的通透酶组成。对所有5885个预测的开放阅读框进行分析,鉴定出186个潜在的MFS蛋白。二元序列比较使其中149个能够聚类为23个家族。可以将假定的通透酶功能赋予12个家族,其中最大的家族包括糖、氨基酸和多药转运。蛋白质的系统发育聚类使我们能够预测总共119种蛋白质可能的通透酶功能。对所有家族进行了多序列比对,并为至少有四个成员的家族构建了进化树。后者导致鉴定出21个可能具有紧密相关通透酶功能的亚簇。对于总共41个聚类或未聚类的蛋白质,未预测到功能线索。