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Title 

Protein NMR structures refined without NOE data

Authors 

Hyojung RyuT R KimSeon Joo AhnSunyoung JiJinhyuk Lee

Publisher 

Public Library of Science

Issue Date 

2014

Citation 

Plos One, vol. 9, no. 10, pp. e108888-e108888

Abstract 

The refinement of low-quality structures is an important challenge in protein structure prediction. Many studies have been conducted on protein structure refinement; the refinement of structures derived from NMR spectroscopy has been especially intensively studied. In this study, we generated flat-bottom distance potential instead of NOE data because NOE data have ambiguity and uncertainty. The potential was derived from distance information from given structures and prevented structural dislocation during the refinement process. A simulated annealing protocol was used to minimize the potential energy of the structure. The protocol was tested on 134 NMR structures in the Protein Data Bank (PDB) that also have X-ray structures. Among them, 50 structures were used as a training set to find the optimal "width" parameter in the flat-bottom distance potential functions. In the validation set (the other 84 structures), most of the 12 quality assessment scores of the refined structures were significantly improved (total score increased from 1.215 to 2.044). Moreover, the secondary structure similarity of the refined structure was improved over that of the original structure. Finally, we demonstrate that the combination of two energy potentials, statistical torsion angle potential (STAP) and the flat-bottom distance potential, can drive the refinement of NMR structures.

ISSN 

1932-6203

Link 

http://dx.doi.org/10.1371/journal.pone.0108888

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2019-05-02


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