Mei B G, Zalkin H
Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907.
J Bacteriol. 1990 Jun;172(6):3512-4. doi: 10.1128/jb.172.6.3512-3514.1990.
A series of deletions was constructed in cloned Escherichia coli purF encoding glutamine phosphoribosylpyrophosphate amidotransferase. These deletions extended into the NH2 terminus of the protein and removed amino acids that are required for glutamine-dependent enzyme activity. Enzyme function, ascribed to the NH3-dependent activity, was retained in deletions that removed up to 237 amino acids. This result supports a model in which PurF-type amidotransferases contain an NH2-terminal glutamine amide transfer domain of approximately 194 to 200 amino acids fused to an aminator domain with NH3-dependent function.
在编码谷氨酰胺磷酸核糖焦磷酸酰胺转移酶的克隆大肠杆菌purF中构建了一系列缺失突变。这些缺失突变延伸到该蛋白质的氨基末端,并去除了谷氨酰胺依赖性酶活性所需的氨基酸。归因于氨依赖性活性的酶功能在去除多达237个氨基酸的缺失突变中得以保留。这一结果支持了一个模型,即PurF型酰胺转移酶包含一个约194至200个氨基酸的氨基末端谷氨酰胺酰胺转移结构域,该结构域与具有氨依赖性功能的氨基化结构域融合。