1. Signaling Pathways
  2. Vitamin D Related/Nuclear Receptor
  3. VKOR

VKOR (维生素 K 环氧化物还原酶)

Vitamin K Epoxide Reductase

维生素 K 环氧化物还原酶 (VKOR) 是一种整合膜蛋白,可催化维生素 K 2,3-环氧化物和维生素 K 还原为维生素 K 氢醌,后者是 γ-谷氨酰羧化反应所需的辅因子。膜拓扑模型显示,VKOR 跨越内质网膜三次,其氨基端位于腔内,羧基端位于细胞质中。活性位点(半胱氨酸 132 和 135)和拟议的华法林结合位点(酪氨酸 139)均位于第三个跨膜螺旋中。 VKOR 是广泛使用的抗凝剂 Warfarin 的靶点,据推测,Warfarin 通过与氧化形式的 VKOR 结合,阻止必需半胱氨酸还原为活性形式,从而发挥作用。VKOR 使用两个半胱氨酸,即 CXXC 氧化还原基序,作为 KO 还原的活性位点。

Vitamin K epoxide reductase (VKOR) is an integral membrane protein that catalyzes the reduction of vitamin K 2,3‐epoxide and vitamin K to vitamin K hydroquinone, a cofactor required for the γ‐glutamyl carboxylation reaction. The membrane topology model shows that VKOR spans the endoplasmic reticulum membrane three times with its amino‐terminus residing in the lumen and the carboxyl‐terminus residing in the cytoplasm. Both the active site (cysteines 132 and 135) and the proposed Warfarin binding site (tyrosine 139) reside in the third transmembrane helix. VKOR is the target of the widely used anticoagulant Warfarin which is proposed to exert its action by binding to the oxidized form of VKOR preventing the reduction of the essential cysteines to its active form. VKOR uses two cysteines, the CXXC redox motif, as the active site for KO reduction[1][2].

VKOR 相关产品 (1):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-14854
    Tecarfarin Antagonist 98.65%
    Tecarfarin (ATI-5923) 是一种具有口服活性,非竞争性维生素 K 环氧化物还原酶 (VKOR) 拮抗剂,损害维生素K依赖性凝血因子 II,VII,IX 和 X 的活化。Tecarfarin具有抗血栓形成活性。
    Tecarfarin