Da Silva Melissa, Shen Ling, Tcherepanov Vasily, Watson Cristalle, Upton Chris
Department of Biochemistry and Microbiology, University of Victoria Petch Building 207, Ring Road, Victoria, BC, V8P 5C2, Canada.
Bioinformatics. 2006 Dec 1;22(23):2846-50. doi: 10.1093/bioinformatics/btl506. Epub 2006 Oct 4.
Of the approximately 200 proteins that have been identified for the vaccinia virus (VACV) genome, many are currently listed as having an unknown function, and seven of these are also found in all other poxvirus genomes that have been sequenced. The G5R protein of VACV is included in this list, and to date, very little is known about this essential and highly conserved protein. Conventional similarity searches of protein databases do not identify significantly similar proteins, and experimental approaches have been unsuccessful at determining protein function.
Using HHsearch, a hidden Markov model (HMM) comparison search tool, the G5R protein was found to be similar to both human and archaeal flap endonucleases (FEN-1) with 96% probability. The G5R protein structure was subsequently successfully modeled using the Robetta protein structure prediction server with an archaeal FEN-1 as the template. The G5R model was then compared to the human FEN-1 crystal structure and was found to be structurally similar to human FEN-1 in both active site residues and DNA substrate binding regions.
在已确定的痘苗病毒(VACV)基因组的约200种蛋白质中,许多目前被列为功能未知,其中七种在所有已测序的其他痘病毒基因组中也有发现。VACV的G5R蛋白就在这份名单中,迄今为止,对这种重要且高度保守的蛋白质了解甚少。对蛋白质数据库进行的常规相似性搜索未发现显著相似的蛋白质,实验方法也未能成功确定该蛋白质的功能。
使用隐藏马尔可夫模型(HMM)比较搜索工具HHsearch,发现G5R蛋白与人类和古细菌 flap 内切核酸酶(FEN-1)相似,概率为96%。随后,以古细菌FEN-1为模板,使用Robetta蛋白质结构预测服务器成功构建了G5R蛋白结构模型。然后将G5R模型与人类FEN-1晶体结构进行比较,发现其在活性位点残基和DNA底物结合区域在结构上均与人类FEN-1相似。