Pegg Scott C-H, Brown Shoshana D, Ojha Sunil, Seffernick Jennifer, Meng Elaine C, Morris John H, Chang Patricia J, Huang Conrad C, Ferrin Thomas E, Babbitt Patricia C
Department of Biopharmaceutical Sciences, University of California, San Francisco, 1700 Fourth Street, San Francisco, California 94143-2250, USA.
Biochemistry. 2006 Feb 28;45(8):2545-55. doi: 10.1021/bi052101l.
The study of mechanistically diverse enzyme superfamilies-collections of enzymes that perform different overall reactions but share both a common fold and a distinct mechanistic step performed by key conserved residues-helps elucidate the structure-function relationships of enzymes. We have developed a resource, the structure-function linkage database (SFLD), to analyze these structure-function relationships. Unique to the SFLD is its hierarchical classification scheme based on linking the specific partial reactions (or other chemical capabilities) that are conserved at the superfamily, subgroup, and family levels with the conserved structural elements that mediate them. We present the results of analyses using the SFLD in correcting misannotations, guiding protein engineering experiments, and elucidating the function of recently solved enzyme structures from the structural genomics initiative. The SFLD is freely accessible at http://sfld.rbvi.ucsf.edu.
对机制多样的酶超家族(即执行不同总体反应但具有共同折叠结构以及由关键保守残基执行的独特机制步骤的酶集合)的研究有助于阐明酶的结构-功能关系。我们开发了一个资源,即结构-功能联系数据库(SFLD),以分析这些结构-功能关系。SFLD的独特之处在于其基于将在超家族、亚组和家族水平上保守的特定部分反应(或其他化学能力)与介导这些反应的保守结构元件相联系的分层分类方案。我们展示了使用SFLD进行分析的结果,包括纠正错误注释、指导蛋白质工程实验以及阐明来自结构基因组学计划的最近解析的酶结构的功能。可通过http://sfld.rbvi.ucsf.edu免费访问SFLD。