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PMID: 18054235 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Fuzzy complexes: polymorphism and structural disorder in protein-protein interactions.

Trends in biochemical sciences ·Vol. 33 ·No. 1 ·2008-01-00 ·Pages 2-8

Tompa P, Fuxreiter M

Abstract

The notion that all protein functions are determined through macromolecular interactions is the driving force behind current efforts that aim to solve the structures of all cellular complexes. Recent findings, however, demonstrate a significant amount of structural disorder or polymorphism in protein complexes, a phenomenon that has been largely overlooked thus far. It is our view that such disorder can be classified into four mechanistic categories, covering a continuous spectrum of structural states from static to dynamic disorder and from segmental to full disorder. To emphasize its generality and importance, we suggest a generic term, 'fuzziness', for this phenomenon. Given the crucial role of protein disorder in protein-protein interactions and in regulatory processes, we envision that fuzziness will become integral to understanding the interactome.

MeSH Terms
Models, Molecular Polymorphism, Genetic Protein Binding Protein Conformation Protein Interaction Mapping Protein Structure, Tertiary Proteins/chemistry,metabolism
Chemicals
Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tompa Peter
Institute of Enzymology, Biological Research Center, Hungarian Academy of Sciences, Budapest, Hungary. tompa@enzim.hu
Fuxreiter Monika
Article Info
Journal
Trends in biochemical sciences
Abbr.
Trends Biochem Sci
ISSN
0968-0004
Published
2008-01-00
Epub
2007-00-28
Pages
2-8
Language
English
Region
England
NLM ID
7610674
Subset
IM
Corrections
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