Institut für organische Chemie und Biochemie, Albert-Ludwigs-Universität Freiburg, D-79104 Freiburg, Germany.
J Mol Biol. 2010 Feb 19;396(2):321-31. doi: 10.1016/j.jmb.2009.11.044. Epub 2009 Nov 23.
The glucosyltransferase Lgt1 is one of three glucosylating toxins of Legionella pneumophila, the causative agent of Legionnaires disease. It acts through specific glucosylation of a serine residue (S53) in the eukaryotic elongation factor 1A and belongs to type A glycosyltransferases. High-resolution crystal structures of Lgt1 show an elongated shape of the protein, with the binding site for uridine disphosphate glucose at the bottom of a deep cleft. Lgt1 shows only a low sequence identity with other type A glycosyltransferases, and structural conservation is limited to a central folding core that is usually observed within this family of proteins. Domains and protrusions added to the core motif represent determinants for the specific recognition and binding of the target. Manual docking experiments based on the crystal structures of toxin and target protein suggest an obvious mode of binding to the target that allows for efficient transfer of a glucose moiety.
Lgt1 糖基转移酶是嗜肺军团菌的三种糖基化毒素之一,嗜肺军团菌是军团病的病原体。它通过对真核延伸因子 1A 中的丝氨酸残基(S53)进行特异性糖基化来发挥作用,属于 A 型糖基转移酶。Lgt1 的高分辨率晶体结构显示出蛋白质的细长形状,其结合部位位于深裂缝底部的尿苷二磷酸葡萄糖。Lgt1 与其他 A 型糖基转移酶的序列同一性较低,结构保守性仅限于通常在该蛋白家族中观察到的中央折叠核心。添加到核心模体的结构域和突出部分是针对靶标的特异性识别和结合的决定因素。基于毒素和靶蛋白晶体结构的手动对接实验表明,存在一种明显的结合靶标的模式,可实现葡萄糖部分的有效转移。