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2000
Volume 12, Issue 2
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

Protein engineering-based studies of the folding transition state have accelerated significantly in the last decade, and more than a half dozen proteins have been subjected to extensive -value analysis. A general picture is emerging from these studies of a transition state in which the large majority of experimentally characterized side chains participate in relatively homogeneous and energetically weak interactions playing only a relatively small role in defining relative folding rates.

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/content/journals/ppl/10.2174/0929866053005809
2005-02-01
2025-06-04
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  • Article Type:
    Review Article
Keyword(s): homogeneous; Protein Folding Transition
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