Conformational and mechanical stability of the isolated large subunit of membrane-bound [NiFe]-hydrogenase from
Gaussian accelerated molecular dynamics
IR spectroscopy
dipole moment
electrostatic potential
hydrogenase
molecular modelling
rigidity profile
size exclusion chromatography
Journal
Frontiers in microbiology
ISSN: 1664-302X
Titre abrégé: Front Microbiol
Pays: Switzerland
ID NLM: 101548977
Informations de publication
Date de publication:
2022
2022
Historique:
received:
18
10
2022
accepted:
23
12
2022
entrez:
3
2
2023
pubmed:
4
2
2023
medline:
4
2
2023
Statut:
epublish
Résumé
Comprising at least a bipartite architecture, the large subunit of [NiFe]-hydrogenase harbors the catalytic nickel-iron site while the small subunit houses an array of electron-transferring Fe-S clusters. Recently, some [NiFe]-hydrogenase large subunits have been isolated showing an intact and redox active catalytic cofactor. In this computational study we have investigated one of these metalloproteins, namely the large subunit HoxG of the membrane-bound hydrogenase from
Identifiants
pubmed: 36733774
doi: 10.3389/fmicb.2022.1073315
pmc: PMC9886862
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1073315Informations de copyright
Copyright © 2023 Dragelj, Karafoulidi-Retsou, Katz, Lenz, Zebger, Caserta, Sacquin-Mora and Mroginski.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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