Stuart Ashley C, Ilyin Valentin A, Sali Andrej
Laboratories of Molecular Biophysics, Pels Family Center for Biochemistry and Structural Biology, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
Bioinformatics. 2002 Jan;18(1):200-1. doi: 10.1093/bioinformatics/18.1.200.
A database comprising all ligand-binding sites of known structure aligned with all related protein sequences and structures is described. Currently, the database contains approximately 50000 ligand-binding sites for small molecules found in the Protein Data Bank (PDB). The structure-structure alignments are obtained by the Combinatorial Extension (CE) program (Shindyalov and Bourne, Protein Eng., 11, 739-747, 1998) and sequence-structure alignments are extracted from the ModBase database of comparative protein structure models for all known protein sequences (Sanchez et al., Nucleic Acids Res., 28, 250-253, 2000). It is possible to search for binding sites in LigBase by a variety of criteria. LigBase reports summarize ligand data including relevant structural information from the PDB file, such as ligand type and size, and contain links to all related protein sequences in the TrEMBL database. Residues in the binding sites are graphically depicted for comparison with other structurally defined family members. LigBase provides a resource for the analysis of families of related binding sites.
描述了一个数据库,该数据库包含所有已知结构的配体结合位点,并与所有相关蛋白质序列和结构进行了比对。目前,该数据库包含蛋白质数据库(PDB)中约50000个小分子的配体结合位点。结构-结构比对通过组合扩展(CE)程序获得(Shindyalov和Bourne,《蛋白质工程》,11,739-747,1998),序列-结构比对从所有已知蛋白质序列的比较蛋白质结构模型的ModBase数据库中提取(Sanchez等人,《核酸研究》,28,250-253,2000)。可以通过多种标准在LigBase中搜索结合位点。LigBase报告总结了配体数据,包括来自PDB文件的相关结构信息,如配体类型和大小,并包含指向TrEMBL数据库中所有相关蛋白质序列的链接。结合位点中的残基以图形方式描绘,以便与其他结构定义的家族成员进行比较。LigBase为相关结合位点家族的分析提供了一个资源。