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Thermodynamic database for protein-nucleic acid interactions (ProNIT).

机译:蛋白质-核酸相互作用的热力学数据库(ProNIT)。

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MOTIVATION: Protein-nucleic acid interactions are fundamental to the regulation of gene expression. In order to elucidate the molecular mechanism of protein-nucleic acid recognition and analyze the gene regulation network, not only structural data but also quantitative binding data are necessary. Although there are structural databases for proteins and nucleic acids, there exists no database for their experimental binding data. Thus, we have developed a Thermodynamic Database for Protein-Nucleic Acid Interactions (ProNIT). RESULTS: We have collected experimentally observed binding data from the literature. ProNIT contains several important thermodynamic data for protein-nucleic acid binding, such as dissociation constant (K(d)), association constant (K(a)), Gibbs free energy change (DeltaG), enthalpy change (DeltaH), heat capacity change (DeltaC(p)), experimental conditions, structural information of proteins, nucleic acids and the complex, and literature information. These data are integrated into a relational database system together with structural and functional information to provide flexible searching facilities by using combinations of various terms and parameters. A www interface allows users to search for data based on various conditions, with different display and sorting options, and to visualize molecular structures and their interactions. AVAILABILITY: ProNIT is freely accessible at the URL http://www.rtc.riken.go.jp/jouhou/pronit/pronit.html.
机译:动机:蛋白质-核酸相互作用是调节基因表达的基础。为了阐明蛋白质-核酸识别的分子机制并分析基因调控网络,不仅需要结构数据,而且还需要定量结合数据。尽管有蛋白质和核酸的结构数据库,但没有有关其实验结合数据的数据库。因此,我们开发了蛋白质-核酸相互作用的热力学数据库(ProNIT)。结果:我们从文献中收集了实验观察到的结合数据。 ProNIT包含蛋白质-核酸结合的一些重要热力学数据,例如解离常数(K(d)),缔合常数(K(a)),吉布斯自由能变化(DeltaG),焓变(DeltaH),热容变化(DeltaC(p)),实验条件,蛋白质,核酸和复合物的结构信息以及文献信息。这些数据与结构和功能信息一起集成到关系数据库系统中,以通过使用各种术语和参数的组合来提供灵活的搜索工具。 www界面允许用户根据各种条件,具有不同的显示和排序选项来搜索数据,并可视化分子结构及其相互作用。可用性:可通过以下网址免费访问ProNIT:http://www.rtc.riken.go.jp/jouhou/pronit/pronit.html。

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