Small-world view of the amino acids that play a key role in protein folding
Top Cited Papers
- 25 June 2002
- journal article
- research article
- Published by American Physical Society (APS) in Physical Review E
- Vol. 65 (6), 061910
- https://doi.org/10.1103/physreve.65.061910
Abstract
We use geometrical considerations to provide a different perspective on the fact that a few selected amino acids, the so-called “key residues,” act as nucleation centers for protein folding. By constructing graphs corresponding to protein structures we show that they have the “small-world” feature of having a limited set of vertices with large connectivity. These vertices correspond to the key residues that play the role of “hubs” in the network of interactions that stabilize the structure of the transition state.Keywords
This publication has 26 references indexed in Scilit:
- Molecular dynamics studies on HIV‐1 protease: Drug resistance and folding pathwaysProteins-Structure Function and Bioinformatics, 2001
- Three key residues form a critical contact network in a protein folding transition stateNature, 2001
- The structure of scientific collaboration networksProceedings of the National Academy of Sciences, 2001
- The roles of stability and contact order in determining protein folding ratesNature Structural & Molecular Biology, 2001
- Classes of small-world networksProceedings of the National Academy of Sciences, 2000
- A surprising simplicity to protein foldingNature, 2000
- Identifying the protein folding nucleus using molecular dynamics 1 1Edited by A. R. FershtJournal of Molecular Biology, 2000
- Diameter of the World-Wide WebNature, 1999
- Collective dynamics of ‘small-world’ networksNature, 1998
- Optimization of rates of protein folding: the nucleation-condensation mechanism and its implications.Proceedings of the National Academy of Sciences, 1995