Easy Not Easy: Comparative Modeling with High-Sequence Identity Templates.

Diego Javier Zea, Elin Teppa, Cristina Marino-Buslje

Journal: Methods in molecular biology (Clifton, N.J.) 2023;2627():83-100

PMID: 36959443

Abstract

Homology modeling is the most common technique to build structural models of a target protein based on the structure of proteins with high-sequence identity and available high-resolution structures. This technique is based on the idea that protein structure shows fewer changes than sequence through evolution. While in this scenario single mutations would minimally perturb the structure, experimental evidence shows otherwise: proteins with high conformational diversity impose a limit of the paradigm of comparative modeling as the same protein sequence can adopt dissimilar three-dimensional structures. These cases present challenges for modeling; at first glance, they may seem to be easy cases, but they have a complexity that is not evident at the sequence level. In this chapter, we address the following questions: Why should we care about conformational diversity? How to consider conformational diversity when doing template-based modeling in a practical way?

© 2023. Springer Science+Business Media, LLC, part of Springer Nature.

Address: Laboratory of Computational and Quantitative Biology, LCQB, UMR 7238 CNRS, IBPS, Sorbonne Université, Paris, France.; Toulouse Biotechnology Institute, TBI, Université de Toulouse, CNRS, INRA, INSA, Toulouse, France.; Fundacion Instituto Leloir, Buenos Aires, Argentina. [email protected].

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