Protein Science
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published online before print August 4, 2004, 10.1110/ps.04713804
Protein Science (2004), 13:2446-2457. Published by Cold Spring Harbor Laboratory Press. Copyright © 2004 The Protein Society
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
ps.04713804v1
13/9/2446    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chang, I.
Right arrow Articles by Maritan, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chang, I.
Right arrow Articles by Maritan, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

What can one learn from experiments about the elusive transition state?

Iksoo Chang1,2, Marek Cieplak1,3, Jayanth R. Banavar1 and Amos Maritan4,5

1 Department of Physics, The Pennsylvania State University, University Park, Pennsylvania 16802, USA
2 National Research Laboratory for Computational Proteomics and Biophysics, Department of Physics, Pusan National University, Pusan 609-735, Korea
3 Institute of Physics, Polish Academy of Sciences, 02-668 Warsaw, Poland
4 INFM and Dipatrimento di Fisica ‘G. Galilei,’ Universitá di Padova, 35131 Padova, Italy
5 The Abdus Salam International Center for Theoretical Physics (ICTP), 34100 Trieste, Italy

(RECEIVED March 1, 2004; FINAL REVISION May 7, 2004; ACCEPTED May 14, 2004)

We present the results of an exact analysis of a model energy landscape of a protein to clarify the idea of the transition state and the physical meaning of the {phi} values determined in protein engineering experiments. We benchmark our findings to various theoretical approaches proposed in the literature for the identification and characterization of the transition state.

Keywords: protein folding; transition state; protein engineering

Article published online ahead of print. Article and publication date are at http://www.proteinscience.org/cgi/doi/10.1110/ps.04713804.


Reprint requests to: Marek Cieplak, Institute of Physics, Polish Academy of Sciences, 02-668 Warsaw, Poland; e-mail: mc{at}ifpan.edu.pl; fax: 48-22-843-0926.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
C. Kim, M. Cheon, M. Kang, and I. Chang
A simple and exact Laplacian clustering of complex networking phenomena: Application to gene expression profiles
PNAS, March 18, 2008; 105(11): 4083 - 4087.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
W. Yu, K. Chung, M. Cheon, M. Heo, K.-H. Han, S. Ham, and I. Chang
Cooperative folding kinetics of BBL protein and peripheral subunit-binding domain homologues
PNAS, February 19, 2008; 105(7): 2397 - 2402.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by The Protein Society.