Dataset Information

Fast and accurate modeling of protein-protein interactions by combining template-interface-based docking with flexible refinement.

ABSTRACT: The similarity between folding and binding led us to posit the concept that the number of protein-protein interface motifs in nature is limited, and interacting protein pairs can use similar interface architectures repeatedly, even if their global folds completely vary. Thus, known protein-protein interface architectures can be used to model the complexes between two target proteins on the proteome scale, even if their global structures differ. This powerful concept is combined with a flexible refinement and global energy assessment tool. The accuracy of the method is highly dependent on the structural diversity of the interface architectures in the template dataset. Here, we validate this knowledge-based combinatorial method on the Docking Benchmark and show that it efficiently finds high-quality models for benchmark complexes and their binding regions even in the absence of template interfaces having sequence similarity to the targets. Compared to "classical" docking, it is computationally faster; as the number of target proteins increases, the difference becomes more dramatic. Further, it is able to distinguish binders from nonbinders. These features allow performing large-scale network modeling. The results on an independent target set (proteins in the p53 molecular interaction map) show that current method can be used to predict whether a given protein pair interacts. Overall, while constrained by the diversity of the template set, this approach efficiently produces high-quality models of protein-protein complexes. We expect that with the growing number of known interface architectures, this type of knowledge-based methods will be increasingly used by the broad proteomics community.

SUBMITTER: Tuncbag N

PROVIDER: S-EPMC7448677 | biostudies-literature | 2012 Apr

REPOSITORIES: biostudies-literature

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Fast and accurate modeling of protein-protein interactions by combining template-interface-based docking with flexible refinement.

Tuncbag Nurcan N Keskin Ozlem O Nussinov Ruth R Gursoy Attila A

Proteins 20120131 4

The similarity between folding and binding led us to posit the concept that the number of protein-protein interface motifs in nature is limited, and interacting protein pairs can use similar interface architectures repeatedly, even if their global folds completely vary. Thus, known protein-protein interface architectures can be used to model the complexes between two target proteins on the proteome scale, even if their global structures differ. This powerful concept is combined with a flexible r ...[more]

PMID: 22275112

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Dataset Information

Fast and accurate modeling of protein-protein interactions by combining template-interface-based docking with flexible refinement.

Publications

Fast and accurate modeling of protein-protein interactions by combining template-interface-based docking with flexible refinement.

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