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
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

Pagination

1351-1360

Auteurs

Nolan Chatron (N)

USC 1233 RS2GP, INRA, VetAgro Sup, Univ Lyon, F-69280 Marcy l'Etoile, France.

Rami Abi Khalil (R)

USC 1233 RS2GP, INRA, VetAgro Sup, Univ Lyon, F-69280 Marcy l'Etoile, France.

Etienne Benoit (E)

USC 1233 RS2GP, INRA, VetAgro Sup, Univ Lyon, F-69280 Marcy l'Etoile, France.

Virginie Lattard (V)

USC 1233 RS2GP, INRA, VetAgro Sup, Univ Lyon, F-69280 Marcy l'Etoile, France.

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Classifications MeSH