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. (C) 2021 Elsevier Ltd. All rights reserved.
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Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Univ Calif San Francisco, Grad Grp Biophys, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Dill, Ken A.
Ozkan, S. Banu
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Arizona State Univ, Dept Phys, Tempe, AZ 85287 USAUniv Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Ozkan, S. Banu
Shell, M. Scott
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Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USAUniv Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
Shell, M. Scott
Weikl, Thomas R.
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Max Planck Inst Colloids & Interfaces, Dept Theory & Biosyst, D-14424 Potsdam, GermanyUniv Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA