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曲霉 N(5)-羧基氨基咪唑核苷酸合成酶的结构与功能研究。

Structural and functional studies of Aspergillus clavatus N(5)-carboxyaminoimidazole ribonucleotide synthetase .

机构信息

Department of Biochemistry, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Biochemistry. 2010 Feb 2;49(4):752-60. doi: 10.1021/bi901599u.

Abstract

N(5)-Carboxyaminoimidazole ribonucleotide synthetase (N(5)-CAIR synthetase), a key enzyme in microbial de novo purine biosynthesis, catalyzes the conversion of aminoimidazole ribonucleotide (AIR) to N(5)-CAIR. To date, this enzyme has been observed only in microorganisms, and thus, it represents an ideal target for antimicrobial drug development. Here we report the cloning, crystallization, and three-dimensional structural analysis of Aspergillus clavatus N(5)-CAIR synthetase solved in the presence of either Mg(2)ATP or MgADP and AIR. These structures, determined to 2.1 and 2.0 A, respectively, revealed that AIR binds in a pocket analogous to that observed for other ATP-grasp enzymes involved in purine metabolism. On the basis of these models, a site-directed mutagenesis study was subsequently conducted that focused on five amino acid residues located in the active site region of the enzyme. These investigations demonstrated that Asp 153 and Lys 353 play critical roles in catalysis without affecting substrate binding. All other mutations affected substrate binding and, in some instances, catalysis as well. Taken together, the structural and kinetic data presented here suggest a catalytic mechanism whereby Mg(2)ATP and bicarbonate first react to form the unstable intermediate carboxyphosphate. This intermediate subsequently decarboxylates to CO(2) and inorganic phosphate, and the amino group of AIR, through general base assistance by Asp 153, attacks CO(2) to form N(5)-CAIR.

摘要

N(5)-羧基咪唑核苷酸合成酶(N(5)-CAIR 合成酶)是微生物从头嘌呤生物合成中的关键酶,可催化氨基咪唑核苷酸(AIR)转化为 N(5)-CAIR。迄今为止,该酶仅在微生物中观察到,因此,它是开发抗菌药物的理想靶标。在此,我们报告了 Aspergillus clavatus N(5)-CAIR 合成酶的克隆、结晶和三维结构分析,该酶分别在存在 Mg(2)ATP 或 MgADP 和 AIR 的情况下进行了分析。这些结构分别解析至 2.1 和 2.0Å,揭示了 AIR 结合在一个类似于其他参与嘌呤代谢的 ATP 捕捉酶的口袋中。基于这些模型,随后进行了定点突变研究,重点研究了位于酶活性部位区域的五个氨基酸残基。这些研究表明,Asp 153 和 Lys 353 在不影响底物结合的情况下对催化起着关键作用。所有其他突变均影响底物结合,在某些情况下还影响催化。总之,这里提出的结构和动力学数据表明了一种催化机制,其中 Mg(2)ATP 和碳酸氢盐首先反应形成不稳定的中间产物羧基磷酸。该中间产物随后脱羧形成 CO(2)和无机磷酸,而 AIR 的氨基通过 Asp 153 的广义碱辅助,攻击 CO(2)形成 N(5)-CAIR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f200/2849000/a52bc9e22b83/nihms168877f1.jpg

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