Périer F, Coulter K L, Liang H, Radeke C M, Gaber R F, Vandenberg C A
Department of Biological Sciences, University of California, Santa Barbara 93106.
FEBS Lett. 1994 Sep 5;351(2):286-90. doi: 10.1016/0014-5793(94)00879-5.
Two suppressors of the growth deficiency of a potassium transport mutant of Saccharomyces cerevisiae were isolated from a mouse cDNA expression library. These suppressors, SKD1 and SKD2 (suppressor of K+ transport growth defect), were cDNAs encoding members of a family of ATPases involved in membrane fusion (N-ethylmaleimide-sensitive fusion protein, NSF), cell division cycle regulation (CDC48p), peroxisome assembly (Pas1p), and transcriptional regulation (TBP-1). The SKD1 protein constitutes a novel member of this family with 49-58% amino acid sequence similarity with other family members, and contains a single ATP binding site. The SKD2 polypeptide is the mouse homolog of NSF.
从一个小鼠cDNA表达文库中分离出了酿酒酵母钾转运突变体生长缺陷的两个抑制子。这些抑制子,即SKD1和SKD2(钾转运生长缺陷抑制子),是编码参与膜融合(N-乙基马来酰亚胺敏感融合蛋白,NSF)、细胞分裂周期调控(CDC48p)、过氧化物酶体组装(Pas1p)和转录调控(TBP-1)的ATP酶家族成员的cDNA。SKD1蛋白构成了该家族的一个新成员,与其他家族成员具有49%-58%的氨基酸序列相似性,并含有一个单一的ATP结合位点。SKD2多肽是NSF的小鼠同源物。