Structural Investigation of the Vitamin K Epoxide Reductase (VKORC1) Binding Site with Vitamin K.
Journal
Biochemistry
ISSN: 1520-4995
Titre abrégé: Biochemistry
Pays: United States
ID NLM: 0370623
Informations de publication
Date de publication:
07 04 2020
07 04 2020
Historique:
pubmed:
18
3
2020
medline:
11
11
2020
entrez:
18
3
2020
Statut:
ppublish
Résumé
The vitamin K epoxide reductase (VKORC1) enzyme is of primary importance in many physiological processes, i.e., blood coagulation, energy metabolism, and arterial calcification prevention, due to its role in the vitamin K cycle. Indeed, VKORC1 catalyzes reduction of vitamin K epoxide to quinone and then to hydroquinone. However, the three-dimensional VKORC1 structure remains experimentally undetermined, because of the endoplasmic reticulum membrane location of this enzyme. Here we present a molecular modeling investigation of the VKORC1 enzymatic site structure and function, supported by
Identifiants
pubmed: 32182040
doi: 10.1021/acs.biochem.9b01084
doi:
Substances chimiques
vitamin K1 oxide
25486-55-9
Vitamin K 1
84-80-0
VKORC1 protein, human
EC 1.17.4.4
Vitamin K Epoxide Reductases
EC 1.17.4.4
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM