Schubot Florian D, Cherry Scott, Austin Brian P, Tropea Joseph E, Waugh David S
Macromolecular Crystallography Laboratory, Center for Cancer Research, National Cancer Institute at Frederick, P.O. Box B, Frederick, MD 21702-1201, USA.
Protein Sci. 2005 Jun;14(6):1679-83. doi: 10.1110/ps.051446405.
Yersinia pestis, the causative agent of the plague, employs a type III secretion system (T3SS) to secrete and translocate virulence factors into to the cytoplasm of mammalian host cells. One of the secreted virulence factors is YopR. Little is known about the function of YopR other than that it is secreted into the extracellular milieu during the early stages of infection and that it contributes to virulence. Hoping to gain some insight into the function of YopR, we determined the crystal structure of its protease-resistant core domain, which consists of residues 38-149 out of 165 amino acids. The core domain is composed of five alpha-helices that display unexpected structural similarity with one domain of YopN, a central regulator of type III secretion in Y. pestis. This finding raises the possibility that YopR may play a role in the regulation of type III secretion.
鼠疫耶尔森菌是鼠疫的病原体,它利用III型分泌系统(T3SS)将毒力因子分泌并转运到哺乳动物宿主细胞的细胞质中。其中一种分泌的毒力因子是YopR。除了在感染早期它被分泌到细胞外环境中且对毒力有贡献外,人们对YopR的功能知之甚少。为了深入了解YopR的功能,我们确定了其抗蛋白酶核心结构域的晶体结构,该结构域由165个氨基酸中的38 - 149位残基组成。核心结构域由五个α螺旋组成,与鼠疫耶尔森菌III型分泌的中央调节因子YopN的一个结构域表现出意想不到的结构相似性。这一发现增加了YopR可能在III型分泌调节中发挥作用的可能性。