Characterizing molecular flexibility by combining least root mean square deviation measures.
least root mean square deviation
rigid motion
structural comparison
structural motif
Journal
Proteins
ISSN: 1097-0134
Titre abrégé: Proteins
Pays: United States
ID NLM: 8700181
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
received:
22
08
2018
revised:
20
12
2018
accepted:
09
01
2019
pubmed:
22
1
2019
medline:
21
4
2020
entrez:
22
1
2019
Statut:
ppublish
Résumé
The root mean square deviation (RMSD) and the least RMSD are two widely used similarity measures in structural bioinformatics. Yet, they stem from global comparisons, possibly obliterating locally conserved motifs. We correct these limitations with the so-called combined RMSD, which mixes independent lRMSD measures, each computed with its own rigid motion. The combined RMSD is relevant in two main scenarios, namely to compare (quaternary) structures based on motifs defined from the sequence (domains and SSE) and to compare structures based on structural motifs yielded by local structural alignment methods. We illustrate the benefits of combined RMSD over the usual RMSD on three problems, namely (a) the assignment of quaternary structures for hemoglobin (scenario #1), (b) the calculation of structural phylogenies (case study: class II fusion proteins; scenario #1), and (c) the analysis of conformational changes based on combined RMSD of rigid structural motifs (case study: one class II fusion protein; scenario #2). Based on these illustrations, we argue that the combined RMSD is a tool of choice to perform positive and negative discrimination of degree of freedom, with applications to the design of move sets and collective coordinates. Executables to compute combined RMSD are available within the Structural Bioinformatics Library (http://sbl.inria.fr).
Substances chimiques
Proteins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
380-389Informations de copyright
© 2019 Wiley Periodicals, Inc.