The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Allostery and cooperativity revisited
Open accessAbstract
Although phenomenlogical models that account for cooperativity in allosteric systems date back to the early and mid‐60's (e.g., the KNF and MWC models), there is resurgent interest in the topic due to the recent experimental and computational studies that attempted to reveal, at an atomistic level, how allostery actually works. In this review, using systems for which atomistic simulations have been carried out in our groups as examples, we describe the current understanding of allostery, how the mechanisms go beyond the classical MWC/Pauling‐KNF descriptions, and point out that the “new view” of allostery, emphasizing “population shifts,” is, in fact, an “old view.” The presentation offers not only an up‐to‐date description of allostery from a theoretical/computational perspective, but also helps to resolve several outstanding issues concerning allostery.
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Cites
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Cited by
The ensemble nature of allostery
Motlagh, H. N., Wrabl, J. O., Li, J., & Hilser, V. J. (2014) · Nature · doi:10.1038/nature13001 · Cited by 1,247
The Molecular Basis of G Protein–Coupled Receptor Activation
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An introduction to NMR-based approaches for measuring protein dynamics
Kleckner, I. R., & Foster, M. P. (2011) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2010.10.012 · Cited by 561
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Protein Allostery and Conformational Dynamics
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Metadata
- Authors
- Cui, Q., & Karplus, M.
- Venue
- Protein Science
- Publisher
- Wiley
- Published
- 2008-08
- Volume
- 17
- Issue
- 8
- Pages
- 1295-1307
- ISSN
- 0961-8368 (ISSN-L)
- 1469-896X
- OpenAlex
- W2115152262
- Cited by
- 681
- References
- 4
- FWCI
- 15.01
- Type
- journal article
- Language
- en
- Open access
- bronze
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