Wolan Dennis W, Cheong Cheom-Gil, Greasley Samantha E, Wilson Ian A
Department of Molecular Biology and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Biochemistry. 2004 Feb 10;43(5):1171-83. doi: 10.1021/bi030162i.
Within de novo purine biosynthesis, the AICAR transformylase and IMP cyclohydrolase activities of the bifunctional enzyme ATIC convert the intermediate AICAR to the final product of the pathway, IMP. Identification of the AICAR transformylase active site and a proposed formyl transfer mechanism have already resulted from analysis of crystal structures of avian ATIC in complex with substrate and/or inhibitors. Herein, we focus on the IMPCH active site and the cyclohydrolase mechanism through comparison of crystal structures of XMP inhibitor complexes of human ATIC at 1.9 A resolution with the previously determined avian enzyme. This first human ATIC structure was also determined to ascertain whether any subtle structural differences, compared to the homologous avian enzyme, should be taken into account for structure-based inhibitor design. These structural comparisons, as well as comparative analyses with other IMP and XMP binding proteins, have enabled a catalytic mechanism to be formulated. The primary role of the IMPCH active site appears to be to induce a reconfiguration of the substrate FAICAR to a less energetically favorable, but more reactive, conformer. Backbone (Arg64 and Lys66) and side chain interactions (Thr67) in the IMPCH active site reorient the 4-carboxamide from the preferred conformer that binds to the AICAR Tfase active site to one that promotes intramolecular cyclization. Other backbone amides (Ile126 and Gly127) create an oxyanion hole that helps orient the formyl group for nucleophilic attack by the 4-carboxamide amine and then stabilize the anionic intermediate. Several other residues, including Lys66, Tyr104, Asp125, and Lys137', provide substrate specificity and likely enhance the catalytic rate through contributions to acid-base catalysis.
在从头嘌呤生物合成过程中,双功能酶ATIC的AICAR转甲酰基酶和IMP环水解酶活性将中间体AICAR转化为该途径的最终产物IMP。通过对与底物和/或抑制剂复合的禽ATIC晶体结构的分析,已经确定了AICAR转甲酰基酶的活性位点和一种假定的甲酰基转移机制。在此,我们通过比较人ATIC与XMP抑制剂复合物在1.9 Å分辨率下的晶体结构与先前确定的禽酶晶体结构,聚焦于IMPCH活性位点和环水解酶机制。还确定了首个人类ATIC结构,以确定与同源禽酶相比,在基于结构的抑制剂设计中是否应考虑任何细微的结构差异。这些结构比较以及与其他IMP和XMP结合蛋白的比较分析,使得能够构建一种催化机制。IMPCH活性位点的主要作用似乎是诱导底物FAICAR重新配置为能量上不太有利但反应性更高的构象异构体。IMPCH活性位点中的主链(Arg64和Lys66)和侧链相互作用(Thr67)将4-羧酰胺从与AICAR Tfase活性位点结合的优选构象重新定向为促进分子内环化的构象。其他主链酰胺(Ile126和Gly127)形成一个氧阴离子洞,有助于将甲酰基定向为被4-羧酰胺胺进行亲核攻击,然后稳定阴离子中间体。其他几个残基,包括Lys66、Tyr104、Asp125和Lys137',提供底物特异性,并可能通过对酸碱催化的贡献来提高催化速率。