Literature DB >> 29605934

Modeling the Structure of Helical Assemblies with Experimental Constraints in Rosetta.

Ingemar André1.   

Abstract

Determining high-resolution structures of proteins with helical symmetry can be challenging due to limitations in experimental data. In such instances, structure-based protein simulations driven by experimental data can provide a valuable approach for building models of helical assemblies. This chapter describes how the Rosetta macromolecular package can be used to model homomeric protein assemblies with helical symmetry in a range of modeling scenarios including energy refinement, symmetrical docking, comparative modeling, and de novo structure prediction. Data-guided structure modeling of helical assemblies with experimental information from electron density, X-ray fiber diffraction, solid-state NMR, and chemical cross-linking mass spectrometry is also described.

Keywords:  Fibers; Fibrils; Helical assemblies; Helical symmetry; Rosetta; Structure determination; Structure prediction

Mesh:

Substances:

Year:  2018        PMID: 29605934     DOI: 10.1007/978-1-4939-7759-8_30

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Structural basis for target site selection in RNA-guided DNA transposition systems.

Authors:  Amy Wei-Lun Tsai; Eshan Mehrotra; Michael T Petassi; Shan-Chi Hsieh; Jung-Un Park; Ailong Ke; Joseph E Peters; Elizabeth H Kellogg
Journal:  Science       Date:  2021-07-15       Impact factor: 63.714

2.  Amyloid β 42 fibril structure based on small-angle scattering.

Authors:  Veronica Lattanzi; Ingemar André; Urs Gasser; Marija Dubackic; Ulf Olsson; Sara Linse
Journal:  Proc Natl Acad Sci U S A       Date:  2021-11-30       Impact factor: 11.205

  2 in total

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