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Flexible structural comparison allowing hinge-bending, swiveling motions

  1. Author:
    Verbitsky, G.
    Nussinov, R.
    Wolfson, H.
  2. Author Address

    Nussinov R NCI, Frederick Canc Res & Dev Ctr, Frederick Canc Res Facil,Lab Expt & Computat Biol, Intramural Res Support Program,SAIC Bldg 469,Room 151 Frederick, MD 21702 USA NCI, Frederick Canc Res & Dev Ctr, Frederick Canc Res Facil,Lab Expt & Computat Biol, Intramural Res Support Program,SAIC Frederick, MD 21702 USA Tel Aviv Univ, Sch Math Sci, Dept Comp Sci IL-69978 Tel Aviv Israel Tel Aviv Univ, Sackler Sch Med, Sackler Inst Mol Med IL-69978 Tel Aviv Israel
    1. Year: 1999
  1. Journal: Proteins
    1. 34
    2. 2
    3. Pages: 232-254
  2. Type of Article: Article
  1. Abstract:

    We present an efficient method for flexible comparison of protein structures, allowing swiveling motions. In all currently available methodologies developed and applied to the comparisons of protein structures, the molecules are considered to be rigid objects. The method described here extends and generalizes current approaches to searches for structural similarity between molecules by vie viewing proteins as objects consisting of rigid parts connected by rotary joints. During the matching, the rigid subparts are allowed to be rotated with respect to each other around swiveling points in one of the molecules, This technique straightforwardly detects structural motifs having hinge(s) between their domains. Whereas other existing methods detect hinge-bent motifs by initially finding the matching rigid parts and subsequently merging these together, our method automatically detects recurring substructures, allowing full 3 dimensional rotations about their swiveling points. Yet the method is extremely fast, avoiding the time-consuming full conformational space search. Comparison of two protein structures, without a predefinition of the motif, takes only seconds to one minute on a workstation per hinge. Hence, the molecule can be scanned for many potential hinge sites, allowing practically all C-alpha atoms to be tried as swiveling points. This algorithm provides a highly efficient, fully automated tool. Its complexity is only O(n(2)), where n is the number of C-alpha atoms in the compared molecules. As in our previous methodologies, the matching is independent of the order of the amino acids in the polypeptide chain. Here Fee illustrate the performance of this highly powerful tool on a large number of proteins exhibiting hinge-bending domain movements. Despite the motions, known hinge-bent domains/motifs which have been assembled and classified, are correctly identified. Additional matches are detected as well. This approach has been motivated by a technique for model based recognition of articulated objects originating in computer vision and robotics. Published 1999 Wiley-Liss, Inc.(dagger) [References: 31]

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