Kean Kelsey M, Codding Sara J, Asamizu Shumpei, Mahmud Taifo, Karplus P Andrew
Department of Biochemistry and Biophysics, Oregon State University , 2011 ALS Building, Corvallis, Oregon 97331-7305, United States.
Biochemistry. 2014 Jul 8;53(26):4250-60. doi: 10.1021/bi5003508. Epub 2014 Jun 25.
Sedoheptulose 7-phosphate cyclases (SH7PCs) encompass three enzymes involved in producing the core cyclitol structures of pseudoglycosides and similar bioactive natural products. One such enzyme is ValA from Streptomyces hygroscopicus subsp. jinggangensis 5008, which makes 2-epi-5-epi-valiolone as part of the biosynthesis of the agricultural antifungal agent validamycin A. We present, as the first SH7PC structure, the 2.1 Å resolution crystal structure of ValA in complex with NAD+ and Zn2+ cofactors. ValA has a fold and active site organization resembling those of the sugar phosphate cyclase dehydroquinate synthase (DHQS) and contains two notable, previously unrecognized interactions between NAD+ and Asp side chains conserved in all sugar phosphate cyclases that may influence catalysis. Because the domains of ValA adopt a nearly closed conformation even though no sugar substrate is present, comparisons with a ligand-bound DHQS provide a model for aspects of substrate binding. One striking active site difference is a loop that adopts a distinct conformation as a result of an Asp→Asn change with respect to DHQS and alters the identity and orientation of a key Arg residue. This and other active site differences in ValA are mostly localized to areas where the ValA substrate differs from that of DHQS. Sequence comparisons with a second SH7PC making a product with distinct stereochemistry lead us to postulate that the product stereochemistry of a given SH7PC is not the result of events taking place during catalysis but is accomplished by selective binding of either the α or β pyranose anomer of the substrate.
景天庚酮糖7-磷酸环化酶(SH7PCs)包含三种参与假糖苷和类似生物活性天然产物核心环醇结构生成的酶。其中一种酶是来自吸水链霉菌井冈亚种5008的ValA,它在农用抗真菌剂井冈霉素A的生物合成过程中合成2-表-5-表-井冈霉醇作为一部分。我们首次报道了ValA与NAD⁺和Zn²⁺辅因子复合物的2.1 Å分辨率晶体结构。ValA的折叠和活性位点组织类似于磷酸糖环化酶脱氢奎尼酸合酶(DHQS),并且在所有磷酸糖环化酶中保守的NAD⁺与Asp侧链之间存在两个显著的、以前未被识别的相互作用,这可能会影响催化作用。由于即使没有糖底物存在,ValA的结构域也采用近乎封闭的构象,因此与结合配体的DHQS进行比较为底物结合的各个方面提供了一个模型。一个显著的活性位点差异是一个环,由于相对于DHQS发生了Asp→Asn的变化,它采用了不同的构象,并改变了一个关键Arg残基的特性和方向。ValA中的这个以及其他活性位点差异大多局限于ValA底物与DHQS底物不同的区域。与另一种产生具有不同立体化学产物的SH7PC进行序列比较,使我们推测给定SH7PC的产物立体化学不是催化过程中发生的事件的结果而是由底物的α或β吡喃糖端基异构体的选择性结合完成的。