首页> 外文期刊>Comparative and functional genomics >Physiological Function of Mycobacterial mtFabD, an Essential Malonyl-CoA:AcpM Transacylase of Type 2 Fatty Acid Synthase FASII, in Yeastmct1ΔCells
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Physiological Function of Mycobacterial mtFabD, an Essential Malonyl-CoA:AcpM Transacylase of Type 2 Fatty Acid Synthase FASII, in Yeastmct1ΔCells

机译:分枝杆菌mtFabD(一种必需的丙二酰辅酶A:AcpM 2型脂肪酸合酶FASII的转酰酶)在Yeastmct1Δ细胞中的生理功能

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Mycobacterium tuberculosismtFabD is an essential malonyl-CoA:AcpM transacylase and is important for vital protein-protein interactions within type 2 fatty acid synthase FASII. mtFabD contacts KasA, KasB, FabH, InhA, and possibly also HadAB, HadBC, and FabG1/MabA. Disruption of mtFabD's interactions during FASII has been proposed for drug development. Here, the gene for a mitochondrially targeted mtFabD was ectopically expressed inSaccharomyces cerevisiaemct1Δmutant cells lacking the corresponding mitochondrial malonyl-CoA transferase Mct1p, allowing the mutants to recover their abilities to respire on glycerol and synthesize lipoic acid. Hence, mtFabD could physiologically function in an environment lacking holo-AcpM or other native interaction partners.
机译:结核分枝杆菌mtFabD是必不可少的丙二酰辅酶A:AcpM转酰酶,对于2型脂肪酸合酶FASII中重要的蛋白质相互作用至关重要。 mtFabD与KasA,KasB,FabH,InhA以及可能的HadAB,HadBC和FabG1 / MabA联系。有人提出在FASII中破坏mtFabD的相互作用来开发药物。在此,针对线粒体靶向的mtFabD的基因在缺少相应线粒体丙二酰-CoA转移酶Mct1p的酿酒酵母中突变表达,从而使这些突变体恢复了在甘油上呼吸和合成硫辛酸的能力。因此,mtFabD可以在缺乏完整AcpM或其他天然相互作用伙伴的环境中生理发挥作用。

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