Bochkarev A, Barwell J A, Pfuetzner R A, Furey W, Edwards A M, Frappier L
Department of Pathology, McMaster University, Hamilton, Ontario, Canada.
Cell. 1995 Oct 6;83(1):39-46. doi: 10.1016/0092-8674(95)90232-5.
The crystal structure of the DNA-binding and dimerization domains of the Epstein-Barr virus nuclear antigen 1 (EBNA1), which binds to and activates DNA replication from the latent origin of replication in Epstein-Barr virus, was solved at 2.5 A resolution. EBNA1 appears to bind DNA via two independent regions termed the core and the flanking DNA-binding domains. The core DNA-binding domain, which comprises both the dimerization domain and a helix predicted to bind the inner portion of the EBNA1 DNA recognition element, was remarkably similar to the structure of the papillomavirus E2 protein, despite a complete lack of sequence conservation. The flanking DNA-binding domain, only a portion of which is contained in the current structure, consists in part of an alpha helix whose N-terminus contacts the outer regions of the EBNA1 DNA recognition element.
爱泼斯坦-巴尔病毒核抗原1(EBNA1)的DNA结合和二聚化结构域可结合并激活爱泼斯坦-巴尔病毒潜伏性复制起点的DNA复制,其晶体结构已在2.5埃分辨率下解析出来。EBNA1似乎通过两个独立区域结合DNA,这两个区域分别称为核心区和侧翼DNA结合结构域。核心DNA结合结构域包含二聚化结构域和一个预测可结合EBNA1 DNA识别元件内部的螺旋结构,尽管完全缺乏序列保守性,但它与乳头瘤病毒E2蛋白的结构非常相似。侧翼DNA结合结构域目前结构中仅包含一部分,部分由一个α螺旋组成,其N端与EBNA1 DNA识别元件的外部区域接触。