Flöckner H, Domingues F S, Sippl M J
Center for Applied Molecular Engineering, University of Salzburg, Austria.
Proteins. 1997;Suppl 1:129-33. doi: 10.1002/(sici)1097-0134(1997)1+<129::aid-prot17>3.3.co;2-f.
We submitted nine predictions to CASP2 using our fold recognition program ProFIT. Two of these structures were still unsolved by the end of the experiment, six had a recognizable fold, and one fold was new. Four predictions of the six recognizable folds were correct. Two models were excellent in terms of alignment quality (T0031, T0004): in one the alignment was partially correct (T0014), and one fold was correctly identified (T0038). We discuss improvements of the program and analyze the prediction results.
我们使用折叠识别程序ProFIT向CASP2提交了9个预测结果。在实验结束时，其中两个结构仍未得到解析，六个具有可识别的折叠，还有一个折叠是新的。六个可识别折叠中的四个预测是正确的。两个模型在比对质量方面表现出色（T0031、T0004）：一个比对部分正确（T0014），一个折叠被正确识别（T0038）。我们讨论了该程序的改进并分析了预测结果。
