| Literature DB >> 34224747 |
Roy Nassar1, Gregory L Dignon2, Rostam M Razban2, Ken A Dill3.
Abstract
The protein folding problem was first articulated as question of how order arose from disorder in proteins: How did the various native structures of proteins arise from interatomic driving forces encoded within their amino acid sequences, and how did they fold so fast? These matters have now been largely resolved by theory and statistical mechanics combined with experiments. There are general principles. Chain randomness is overcome by solvation-based codes. And in the needle-in-a-haystack metaphor, native states are found efficiently because protein haystacks (conformational ensembles) are funnel-shaped. Order-disorder theory has now grown to encompass a large swath of protein physical science across biology.Entities:
Keywords: coarse-grained modeling; disordered proteins; protein aggregation; protein folding theory; statistical mechanics
Mesh:
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Year: 2021 PMID: 34224747 PMCID: PMC8547331 DOI: 10.1016/j.jmb.2021.167126
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 6.151