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Structural characterization of AtmS13 a putative sugar aminotransferase involved in indolocarbazole AT2433 aminopentose biosynthesis

机译:AtmS13的结构表征一种可能的糖氨基转移酶涉及吲哚并咔唑AT2433氨基戊糖的生物合成

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摘要

AT2433 from Actinomadura melliaura is an indolocarbazole antitumor antibiotic structurally distinguished by its unique aminodideoxypentose-containing disaccharide moiety. The corresponding sugar nucleotide-based biosynthetic pathway for this unusual sugar derives from comparative genomics where AtmS13 has been suggested as the contributing sugar aminotransferase (SAT). Determination of the AtmS13 X-ray structure at 1.50 Å resolution reveals it as a member of the aspartate aminotransferase fold type I (AAT-I). Structural comparisons of AtmS13 with homologous SATs that act upon similar substrates implicate potential active site residues that contribute to distinctions in sugar C5 (hexose versus pentose) and/or sugar C2 (deoxy versus hydroxyl) substrate specificity.
机译:来自Actinomadura melliaura的AT2433是一种吲哚并咔唑抗肿瘤抗生素,其结构独特之处在于其独特的含氨基二甲氧基戊糖的二糖部分。这种不寻常糖的相应的基于糖核苷酸的生物合成途径来自比较基因组学,其中AtmS13被认为是贡献性糖氨基转移酶(SAT)。确定AtmS13 X射线结构的分辨率为1.50Å,表明它是I型天冬氨酸氨基转移酶折叠(AAT-1)的成员。 AtmS13与作用于相似底物的同源SAT的结构比较表明,潜在的活性位点残基有助于糖C5(己糖与戊糖)和/或糖C2(脱氧与羟基)底物特异性的区别。

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