Olechnovič Kliment, Banciul Rita, Dapkūnas Justas, Venclovas Česlovas
Institute of Biotechnology, Life Sciences Center, Vilnius University, Vilnius, Lithuania.
Université Grenoble Alpes, CNRS, Grenoble INP, LJK, Grenoble, France.
Proteins. 2025 Jan 2. doi: 10.1002/prot.26792.
FTDMP is a software framework for biomolecular docking and scoring. It can perform docking of subunits containing one or more protein, DNA, or RNA chains, followed by subsequent scoring of the resulting models. FTDMP can also be used for the ranking of user-provided models of biomolecular complexes, generated by any structure prediction method. FTDMP evaluates models according to the consensus-based method VoroIF-jury, which combines individual scores derived from the Voronoi tessellation of biomolecular structures. In addition to the default scoring mode, FTDMP can easily adopt additional scores; thus, it may be used as a tool to assess newly developed scoring functions. FTDMP was evaluated during blind testing in recent CAPRI experiments and using protein-protein, protein-DNA, and protein-RNA docking benchmarks. It proved to be a useful tool for different research tasks, related to modeling biomolecular interactions. The software, cleaned docking benchmarks, and benchmarking results are available at https://bioinformatics.lt/software/ftdmp/.
FTDMP是一个用于生物分子对接和评分的软件框架。它可以对包含一条或多条蛋白质、DNA或RNA链的亚基进行对接,然后对所得模型进行评分。FTDMP还可用于对通过任何结构预测方法生成的用户提供的生物分子复合物模型进行排序。FTDMP根据基于共识的方法VoroIF-jury评估模型,该方法结合了从生物分子结构的Voronoi镶嵌得出的个体分数。除了默认的评分模式外,FTDMP还可以轻松采用其他分数;因此,它可以用作评估新开发的评分函数的工具。在最近的CAPRI实验的盲测中以及使用蛋白质-蛋白质、蛋白质-DNA和蛋白质-RNA对接基准对FTDMP进行了评估。事实证明,它是用于与生物分子相互作用建模相关的不同研究任务的有用工具。该软件、清理后的对接基准和基准测试结果可在https://bioinformatics.lt/software/ftdmp/上获取。