Rational redesign of bacterialS-adenosylmethionine-synthase by 3D-modelling and docking led to variants that allow synthesis of methylation cofactor SAM (AdoMet) without product inhibition, and of higher alkyl homologues.
通过三维建模和对接,对细菌
腺苷甲
硫氨酸合成酶进行合理重设计,导致产生变种,可以合成甲基化辅酶S
AM(AdoMet)而无产物抑制,并且可以合成更高级的烷基同系物。