Published May 3, 2017 | Version v1
Conference paper Open

SHREC'17 Track: Protein Shape Retrieval

  • 1. Complex Systems Division, Beijing Computational Science Research Center, Z-Park II, Haidian, Beijing, China 100193
  • 2. Laboratoire GBA EA4627, Conservatoire National des Arts et Métiers, 2 rue Conté, 75003 Paris, France
  • 3. Department of Computer Science, Purdue University, 305 N. University St., West Lafayette, IN 47907, USA
  • 4. Department of Biological Sciences, Purdue University, 249 S. Martin Jischke Dr., West Lafayette, IN 47907, USA
  • 5. Laboratoire CEDRIC EA4647, Conservatoire National des Arts et Métiers, 2 rue Conté, 75003, Paris, France
  • 6. Computer Science Dept., Stony Brook University, Stony Brook, NY 11794, USA

Description

The large number of protein structures deposited in the protein database provide an opportunity to examine the structure relations using computational algorithms, which can be used to classify the structures based on shape similarity. In this paper, we report the result of the SHREC 2017 track on shape retrievals from protein database. The goal of this track is to test the performance of the algorithms proposed by participants for the retrieval of bioshape (proteins). The test set is composed of 5,854 abstracted shapes from actual protein structures after removing model redundancy. Ten query shapes were selected from a set of representative molecules that have important biological functions. Six methods from four teams were evaluated and the performance is summarized in this report, in which both the retrieval accuracy and computational speed were compared. The biological relevance of the shape retrieval approaches is discussed. We also discussed the future perspectives of shape retrieval for biological molecular models.

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Funding

VIDOCK – 2D Conformal mapping of protein surfaces: applications to VIsualization and DOCKing software 640283
European Commission