Skip Navigation



PEDS Advance Access published online on October 24, 2005

Protein Engineering Design and Selection, doi:10.1093/protein/gzi068
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
18/12/597    most recent
gzi068v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Hur, O.
Right arrow Articles by Karplus, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hur, O.
Right arrow Articles by Karplus, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2005. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org
Received August 17, 2005
Accepted September 8, 2005

Article

Methods of translating NMR proton distances into their corresponding heavy atom distances for protein structure prediction with limited experimental data

Oscar Hur 1* and Kevin Karplus 2

1 PO Box 2548, Sunnyvale, CA 94087-0548, USA
2 Department of Biomolecular Engineering, University of California at Santa Cruz, Santa Cruz, CA 95064, USA

* To whom correspondence should be addressed.
Oscar Hur, E-mail: ohur1688{at}alumni.ucsd.edu


   Abstract

This paper proposes a strategy to translate experimental 1H NMR proton distance restraints into their corresponding heavy atom distance restraints for the purpose of protein structure prediction. The relationships between interproton distances and the corresponding heavy atom distances are determined by studying well-resolved X-ray protein structures. The data from the interproton distances of amide protons, {alpha}-protons, {beta}-protons and side chain methyl protons are plotted against the corresponding heavy atoms in scatter plots and then fitted with linear equations for lower bounds, upper bounds and optimal fits. We also transform the scatter plots into two-dimensional heat maps and three-dimensional histograms, which identify the regions where data points concentrate. The common interproton distances between amide protons, {alpha}-protons, {beta}-protons in {alpha}-helices, anti-parallel {beta}-sheets and parallel {beta}-sheets are also tabulated. We have found several patterns emerging from the distance relationships between heavy atom pairs and their corresponding proton pairs. All our upper bound, lower bound and optimal fit results for translating the interproton distance into their corresponding heavy atom distances are tabulated.

Keywords: heavy atom distance; NMR; proton distance.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.