Gaudry M, Bory S, Dubois J, Azerad R, Marquet A
Biochem Biophys Res Commun. 1983 Jun 15;113(2):454-61. doi: 10.1016/0006-291x(83)91747-3.
Two pentapeptides Phe-Leu-X-Glu-Val where X is either the L-threo-gamma-methylglutamic acid or the L-erythro isomer have been synthesized and tested as substrates in the vitamin K dependent carboxylation. The gamma-methylglutamic residue is not carboxylated and both peptides are inhibitors of the carboxylation of the reference peptide Phe-Leu-Glu-Glu-Val. The threo containing isomer has a much better affinity than the reference and is the best inhibitor of this reaction described so far.
合成了两种五肽Phe-Leu-X-Glu-Val,其中X为L-苏式-γ-甲基谷氨酸或L-赤藓糖异构体,并将其作为维生素K依赖性羧化反应的底物进行了测试。γ-甲基谷氨酸残基未被羧化,且两种肽均为参比肽Phe-Leu-Glu-Glu-Val羧化反应的抑制剂。含苏式异构体的肽比参比肽具有更好的亲和力,是迄今为止所描述的该反应的最佳抑制剂。