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      ReSMAP: Web Server for Predicting Residue-Specific Membrane-Association Propensities of Intrinsically Disordered Proteins.

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          Abstract

          The functional processes of many proteins involve the association of their intrinsically disordered regions (IDRs) with acidic membranes. We have identified the membrane-association characteristics of IDRs using extensive molecular dynamics (MD) simulations and validated them with NMR spectroscopy. These studies have led to not only deep insight into functional mechanisms of IDRs but also to intimate knowledge regarding the sequence determinants of membrane-association propensities. Here we turned this knowledge into a web server called ReSMAP, for predicting the residue-specific membrane-association propensities from IDR sequences. The membrane-association propensities are calculated from a sequence-based partition function, trained on the MD simulation results of seven IDRs. Robustness of the prediction is demonstrated by leaving one IDR out of the training set. We anticipate there will be many applications for the ReSMAP web server, including rapid screening of IDR sequences for membrane association.

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          Author and article information

          Journal
          Membranes (Basel)
          Membranes
          MDPI AG
          2077-0375
          2077-0375
          Aug 11 2022
          : 12
          : 8
          Affiliations
          [1 ] Department of Chemistry, University of Illinois at Chicago, Chicago, IL 60607, USA.
          [2 ] Department of Physics, University of Illinois at Chicago, Chicago, IL 60607, USA.
          Article
          membranes12080773
          10.3390/membranes12080773
          9416665
          36005688
          5a5ec3ad-9f52-4a32-956d-05020f08a9af
          History

          membrane-association propensity,intrinsically disordered proteins,intrinsically disordered regions,membrane binding,amphipathic helix

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