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Bacteriophage-encoded glucosyltransferase GtrII of Shigella flexneri: membrane topology and identification of critical residues

机译:弗氏志贺氏菌细菌噬菌体编码的葡萄糖基转移酶GtrII:膜拓扑结构和关键残基的鉴定

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pThe iShigella flexneri/i serotypes differ in the nature of their O-antigens. The addition of glucosyl or O-acetyl groups to the common backbone repeat units gives rise to the different serotypes. GtrII glucosylates rhamnose III of the O-antigen repeat unit, thus converting serotype Y (which has no modifications to the basic O-antigen repeat unit) into serotype 2a, the most prevalent serotype. In the present study, the topology of GtrII has been determined. GtrII has nine transmembrane helices, a re-entrant loop and three large periplasmic regions. Four critical residues (Glusup40/sup, Phesup414/sup, Cyssup435/sup and Lyssup478/sup) were identified in two of the periplasmic regions. Despite the lack of sequence similarity between GtrII and the Gtrs from other serotypes, three of the critical residues identified are conserved in the remaining Gtrs. This is consistent with some degree of mechanistic conservation in this functionally related group of proteins./p
机译:>弗氏志贺氏菌血清型的O抗原性质不同。将葡糖基或O-乙酰基加到共同的骨架重复单元上产生不同的血清型。 GtrII葡萄糖基化O抗原重复单元的鼠李糖III,从而将血清型Y(对基本O抗原重复单元没有修饰)转化为最普遍的血清型2a。在本研究中,已经确定了GtrII的拓扑。 GtrII具有九个跨膜螺旋,一个凹角环和三个大的周质区域。在其中两个中鉴定出四个关键残基(Glu 40 ,Phe 414 ,Cys 435 和Lys 478 )。周质区域。尽管GtrII与其他血清型的Gtrs之间缺乏序列相似性,但鉴定出的三个关键残基在其余的Gtrs中是保守的。这与这组功能相关的蛋白质在一定程度上的机制保守性相符。

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