Capítulo de Libro

Exploring Protein Conformational Diversity

Monzon, Alexander Miguel ; Fornasari, Maria Silvina Icon; Zea, Diego Javier Icon; Parisi, Gustavo Daniel Icon

Otros responsables

Fecha

2019

Editorial

Springer

Revista

Título del libro

Computational Methods in Protein Evolution

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

eISSN

ISBN

978-1-4939-8735-1

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

The native state of proteins is composed of conformers in dynamical equilibrium. In this chapter, different issues related to conformational diversity are explored using a curated and experimentally based database called CoDNaS (Conformational Diversity in the Native State). This database is a collection of redundant structures for the same sequence. CoDNaS estimates the degree of conformational diversity using different global and local structural similarity measures. It allows the user to explore how structural differences among conformers change as a function of several structural features providing further biological information. This chapter explores the measurement of conformational diversity and its relationship with sequence divergence. Also, it discusses how proteins with high conformational diversity could affect homology modeling techniques.

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Licencia Creative Commons

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