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通过phoA融合分析对大肠杆菌α-酮戊二酸通透酶的膜拓扑模型

Membrane topology model of Escherichia coli alpha-ketoglutarate permease by phoA fusion analysis.

作者信息

Seol W, Shatkin A J

机构信息

Center for Advanced Biotechnology and Medicine, Piscataway, New Jersey 08854-5638.

出版信息

J Bacteriol. 1993 Jan;175(2):565-7. doi: 10.1128/jb.175.2.565-567.1993.

Abstract

Escherichia coli alpha-ketoglutarate permease (KgtP) is a 432-amino-acid protein that symports alpha-ketoglutarate and protons. KgtP was predicted to contain 12 membrane-spanning domains on the basis of a calculated hydropathy profile. The membrane topology model of KgtP was analyzed by using kgtP-phoA gene fusions and measuring alkaline phosphatase activities in cells expressing the chimeric proteins. Comparisons of the phosphatase activity levels and the locations of the KgtP-PhoA junctions are consistent with the predicted membrane topology model of KgtP.

摘要

大肠杆菌α-酮戊二酸通透酶(KgtP)是一种由432个氨基酸组成的蛋白质,它协同转运α-酮戊二酸和质子。根据计算得出的亲水性图谱预测,KgtP含有12个跨膜结构域。通过使用kgtP-phoA基因融合体并测量表达嵌合蛋白的细胞中的碱性磷酸酶活性,对KgtP的膜拓扑模型进行了分析。磷酸酶活性水平和KgtP-PhoA连接点位置的比较与预测的KgtP膜拓扑模型一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed3b/196175/4bd806149707/jbacter00044-0272-a.jpg

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