Literature DB >> 14517969

Functional motions can be extracted from on-lattice construction of protein structures.

Pemra Doruker1, Robert L Jernigan.   

Abstract

The three-dimensional structure of a 1509-residue protein-hemagglutinin is reconstructed on a simple cubic lattice by retaining all lattice sites that fall within close proximity of the X-ray coordinates. Coarse-grained normal modes analysis is performed using these lattice sites as the nodes of an elastic network. The collective deformations of the protein can still be extracted from such a structure that just mimics the overall shape of the protein but not its mass distribution. These results emphasize that the overall shape rather than the details of the protein fold determines the dynamical domains in proteins. Thus, low-resolution protein structures, even those constructed on a regularly spaced lattice, can provide insights about the functionally important global dynamics around the native state. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 14517969     DOI: 10.1002/prot.10486

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  19 in total

1.  On the use of low-frequency normal modes to enforce collective movements in refining macromolecular structural models.

Authors:  Marc Delarue; Philippe Dumas
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-19       Impact factor: 11.205

2.  Models to Approximate the Motions of Protein Loops.

Authors:  Aris Skliros; Robert L Jernigan; Andrzej Kloczkowski
Journal:  J Chem Theory Comput       Date:  2010-10-12       Impact factor: 6.006

3.  The role of shape in determining molecular motions.

Authors:  Mingyang Lu; Jianpeng Ma
Journal:  Biophys J       Date:  2005-07-29       Impact factor: 4.033

4.  Packing regularities in biological structures relate to their dynamics.

Authors:  Robert L Jernigan; Andrzej Kloczkowski
Journal:  Methods Mol Biol       Date:  2007

5.  Close correspondence between the motions from principal component analysis of multiple HIV-1 protease structures and elastic network modes.

Authors:  Lei Yang; Guang Song; Alicia Carriquiry; Robert L Jernigan
Journal:  Structure       Date:  2008-02       Impact factor: 5.006

6.  The Extent of Cooperativity of Protein Motions Observed with Elastic Network Models Is Similar for Atomic and Coarser-Grained Models.

Authors:  Taner Z Sen; Yaping Feng; John V Garcia; Andrzej Kloczkowski; Robert L Jernigan
Journal:  J Chem Theory Comput       Date:  2006       Impact factor: 6.006

7.  Predicting the complex structure and functional motions of the outer membrane transporter and signal transducer FecA.

Authors:  Taner Z Sen; Margaret Kloster; Robert L Jernigan; Andrzej Kolinski; Janusz M Bujnicki; Andrzej Kloczkowski
Journal:  Biophys J       Date:  2008-01-04       Impact factor: 4.033

8.  Application of elastic network models to proteins in the crystalline state.

Authors:  Demian Riccardi; Qiang Cui; George N Phillips
Journal:  Biophys J       Date:  2009-01       Impact factor: 4.033

9.  Sequence-specific dynamic information in proteins.

Authors:  H A Scheraga; S Rackovsky
Journal:  Proteins       Date:  2019-06-11

10.  Structural compliance: A new metric for protein flexibility.

Authors:  Domenico Scaramozzino; Pranav M Khade; Robert L Jernigan; Giuseppe Lacidogna; Alberto Carpinteri
Journal:  Proteins       Date:  2020-07-14
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