Comparison of the Intrinsic Dynamics of Proteins Involved in Metabolic Pathways Using Coarse-Grained Normal Mode Analysis

dc.contributor.advisorHati, Sanchita
dc.contributor.authorBretl, Sarah
dc.contributor.authorMcMunn, Ryan
dc.date.accessioned2016-02-26T20:32:24Z
dc.date.available2016-02-26T20:32:24Z
dc.date.issued2015-04
dc.descriptionColor poster with text, images, charts, and graphs.en
dc.description.abstractProtein dynamics play an important role in molecular recognition and catalysis. Each protein structure has unique dynamics encoded by its primary sequence. The collective intrinsic dynamics of a protein, which is defined by its overall architecture, is important in promoting a pre-organized active site conformation that is conducive to molecular recognition and effective catalysis. In an attempt to classify proteins based on their intrinsic dynamics, we are investigating the intrinsic dynamics of enzymes involved in primary metabolic pathways.en
dc.description.sponsorshipUniversity of Wisconsin--Eau Claire Office of Research and Sponsored Programs.en
dc.identifier.urihttp://digital.library.wisc.edu/1793/74150
dc.language.isoen_USen
dc.relation.ispartofseriesUSGZE AS589en
dc.subjectEnzymesen
dc.subjectProtein dynamicsen
dc.subjectProteinsen
dc.titleComparison of the Intrinsic Dynamics of Proteins Involved in Metabolic Pathways Using Coarse-Grained Normal Mode Analysisen
dc.typePresentationen

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