Johnson G, Wu T T
Departments of Biochemistry, Molecular Biology and Cell Biology, and Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA.
Nucleic Acids Res. 2001 Jan 1;29(1):205-6. doi: 10.1093/nar/29.1.205.
The Kabat Database was initially started in 1970 to determine the combining site of antibodies based on the available amino acid sequences. The precise delineation of complementarity determining regions (CDR) of both light and heavy chains provides the first example of how properly aligned sequences can be used to derive structural and functional information of biological macromolecules. This knowledge has subsequently been applied to the construction of artificial antibodies with prescribed specificities, and to many other studies. The Kabat database now includes nucleotide sequences, sequences of T cell receptors for antigens (TCR), major histocompatibility complex (MHC) class I and II molecules, and other proteins of immunological interest. While new sequences are continually added into this database, we have undertaken the task of developing more analytical methods to study the information content of this collection of aligned sequences. New examples of analysis will be illustrated on a yearly basis. The Kabat Database and its applications are freely available at http://immuno.bme.nwu.edu.
卡巴特数据库最初创建于1970年,旨在根据可用的氨基酸序列确定抗体的结合位点。轻链和重链互补决定区(CDR)的精确描绘提供了第一个示例,展示了如何利用正确比对的序列来推导生物大分子的结构和功能信息。这一知识随后被应用于构建具有特定特异性的人工抗体以及许多其他研究。卡巴特数据库现在包括核苷酸序列、抗原T细胞受体(TCR)序列、主要组织相容性复合体(MHC)I类和II类分子,以及其他具有免疫学意义的蛋白质。虽然新序列不断添加到该数据库中,但我们已承担起开发更多分析方法以研究这一比对序列集合信息内容的任务。每年都会举例说明新的分析示例。卡巴特数据库及其应用可在http://immuno.bme.nwu.edu免费获取。