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Eugene I. Shakhnovich

Researcher at Harvard University

Publications -  473
Citations -  26389

Eugene I. Shakhnovich is an academic researcher from Harvard University. The author has contributed to research in topics: Protein folding & Folding (chemistry). The author has an hindex of 82, co-authored 454 publications receiving 24773 citations. Previous affiliations of Eugene I. Shakhnovich include University of Pennsylvania & Russian Academy of Sciences.

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Modeling the kinetics of acylation of insulin using a recursive method for solving the systems of coupled differential equations.

TL;DR: A theoretical method for solving systems of coupled differential equations that describe the kinetics of complicated reaction networks in which a molecule having multiple reaction sites reacts irreversibly with multiple equivalents of a ligand (reagent).
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Disordered heteropolymers with cross-links – phase diagram and conformational transitions

TL;DR: In this paper, replica field theory is used to predict the phase structure of globular random heteropolymers with quenched cross-links, and the cross-link formation is attributed to micro-phase separation of the pre-gel state with crosslinks forming at the microphase interfaces, followed by a second-order transition to a sequence-stabilized globular state.
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Improvisation in evolution of genes and genomes: whose structure is it anyway?

TL;DR: Emerging synergism between data and modeling provides first robust answers to the evolution of complex systems and organisms on all scales--from sequences to organisms and populations.
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Excluded Volume in Protein Sidechain Packing

TL;DR: In this paper, the authors examined the relationship between sidechain geometry and sidechain packing, using an all-atom Monte Carlo simulation to sample the large space of sidechain conformations, and found that excluded volume constraints reduce the size of conformational space by many orders of magnitude, the number of allowed conformations is still large.
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Orientational ordering in sequence-disordered liquid crystalline polymers

TL;DR: In this article, the nematic/isotropic (N/I) phase diagram and orientational ordering in heteropolymers consisting of stiff and flexible segments by field theory was studied. And it was shown that a finite and small variance in sequence disorder is sufficient to destroy orientation ordering; in the lyotropic case, the presence of sequence disorder triples the coexistence density difference compared with that of stiff homopolymers at similar conditions.