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Reyes-Espinosa, F.* ; Juárez-Saldivar, A.* ; Palos, I.* ; Herrera-Mayorga, V.* ; Garcia Perez, C. ; Rivera, G.*

In silico analysis of homologous heterodimers of cruzipain-chagasin from structural models built by homology.

Int. J. Mol. Sci. 20:1320 (2019)
Verlagsversion DOI
Open Access Gold
Creative Commons Lizenzvertrag
The present study gives an overview of the binding energetics of the homologous heterodimers of cruzipain-chagasin based on the binding energy (Delta G(b)) prediction obtained with FoldX. This analysis involves a total of 70 homologous models of the cruzipain-chagasin complex which were constructed by homology from the combinatory variation of nine papain-like cysteine peptidase structures and seven cysteine protease inhibitor structures (as chagasin-like and cystatin-like inhibitors). Only 32 systems have been evaluated experimentally, Delta G(b)(experimental) values previously reported. Therefore, the result of the multiple analysis in terms of the thermodynamic parameters, are shown as relative energy |Delta Delta G| = |Delta G(b)(from) (FoldX) - Delta G(b)(experimental)|. Nine models were identified that recorded |Delta Delta G| < 1.3, five models to 2.8 > |Delta Delta G| > 1.3 and the other 18 models, values of |Delta Delta G| > 2.8. The energetic analysis of the contribution of Delta H and Delta S to Delta G(b) to the 14-molecular model presents a Delta G(b) mostly Delta H-driven at neutral pH and at an ionic strength (I) of 0.15 M. The dependence of Delta G(b)(I,pH) at 298 K to the cruzipain-chagasin complex predicts a linear dependence of Delta G(b)(I). The computational protocol allowed the identification and prediction of thermodynamics binding energy parameters for cruzipain-chagasin-like heterodimers.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Cruzipain ; Chagasin-like ; Cystatin-like ; Molecular Modelling ; Trypanosoma Cruzi; Cysteine Proteinases; Inhibitor Chagasin; Trypanosoma-cruzi; Crystal-structure; Web Server; Cystatin; Protease; Complex; Tool; Evolution
ISSN (print) / ISBN 1422-0067
e-ISSN 1661-6596
Quellenangaben Band: 20, Heft: 6, Seiten: , Artikelnummer: 1320 Supplement: ,
Verlag MDPI
Verlagsort Basel
Begutachtungsstatus Peer reviewed