Horst Jeremy, Samudrala Ram
F1000 Biol Rep. 2009 Sep 8;1:69. doi: 10.3410/B1-69.
We examine the ability of current state-of-the-art methods in protein structure prediction to discriminate topologically distant folds encoded by highly similar (>90% sequence identity) designed proteins in blind protein structure prediction experiments. We detail the corresponding prognosis for the protein fold recognition field and highlight the features of the methodologies that successfully deciphered this folding riddle.
我们在盲蛋白结构预测实验中,检验了当前蛋白质结构预测领域最先进方法,对由高度相似(序列同一性>90%)的设计蛋白编码的拓扑距离较远的折叠进行区分的能力。我们详细阐述了蛋白质折叠识别领域的相应预测,并突出了成功破解这一折叠谜题的方法的特点。