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MmMVK- 3 Crystal structure of MmMVK-mevalonate complex and mevalonate kinase mutants resistant to substrate inhibition

机译:MmMVK-3耐底物抑制的MmMVK-甲羟戊酸酯复合物和甲羟戊酸激酶突变体的晶体结构

摘要

The present invention relates to a 3D crystal structure of MmMVK-mevalonate composite and a substrate inhibition resistant mutant mevalonate kinase (MmMVK). The inventor of the present invention crystal-analyzed a 3D structure of archaea evalonate kinase proteins and mevalonate composite, a substrate, by an X-ray crystallography. In the 3D structure, a second substrate binding site different from currently known substrate binding site is found. When amino acid residue of the novel binding site is mutated, a mutant protein having a resistance to a self-inhibition for inhibiting enzyme activities according to a substrate concentration is found. The present invention determines an enzyme activity analysis of mutant proteins and a 3D structure. A newly developed mutant mevalonate kinase protein would help improve isoprene biosynthesis yield as an enzyme of rate determining step of isoprene biosynthesis in a mevalonate pathway, an isoprene biosynthesis pathway.
机译:本发明涉及MmMVK-甲羟戊酸复合物的3D晶体结构和抗底物抑制性的甲羟戊酸激酶(MmMVK)。本发明的发明人通过X射线晶体学对古生的evalonate激酶蛋白和甲羟戊酸酯复合物(底物)的3D结构进行了晶体分析。在3D结构中,发现了不同于当前已知的底物结合位点的第二底物结合位点。当新的结合位点的氨基酸残基突变时,发现了根据底物浓度具有抑制自抑制酶活性的自抑制性的突变蛋白。本发明确定了突变蛋白和3D结构的酶活性分析。作为在异戊二烯生物合成途径的甲羟戊酸途径中异戊二烯生物合成的速率确定步骤的酶,一种新开发的突变体甲羟戊酸激酶蛋白将有助于提高异戊二烯生物合成的产量。

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