Goyal Kshama, Mohanty Debasisa, Mande Shekhar C
Centre for DNA Fingerprinting and Diagnostics, ECIL Road, Nacharam, Hyderabad 500 076, India.
Nucleic Acids Res. 2007 Jul;35(Web Server issue):W503-5. doi: 10.1093/nar/gkm252. Epub 2007 May 3.
PAR-3D (http://sunserver.cdfd.org.in:8080/protease/PAR_3D/index.html) is a web-based tool that exploits the fact that relative juxtaposition of active site residues is a conserved feature in functionally related protein families. The server uses previously calculated and stored values of geometrical parameters of a set of known proteins (training set) for prediction of active site residues in a query protein structure. PAR-3D stores motifs for different classes of proteases, the ten glycolytic pathway enzymes and metal-binding sites. The server accepts the structures in the pdb format. The first step during the prediction is the extraction of probable active site residues from the query structure. Spatial arrangement of the probable active site residues is then determined in terms of geometrical parameters. These are compared with stored geometries of the different motifs. Its speed and efficiency make it a beneficial tool for structural genomics projects, especially when the biochemical function of the protein has not been characterized.
PAR - 3D(http://sunserver.cdfd.org.in:8080/protease/PAR_3D/index.html)是一个基于网络的工具,它利用了活性位点残基的相对并列在功能相关蛋白质家族中是一个保守特征这一事实。该服务器使用一组已知蛋白质(训练集)的几何参数的先前计算和存储值来预测查询蛋白质结构中的活性位点残基。PAR - 3D存储不同类别的蛋白酶、十种糖酵解途径酶和金属结合位点的基序。该服务器接受pdb格式的结构。预测过程的第一步是从查询结构中提取可能的活性位点残基。然后根据几何参数确定可能的活性位点残基的空间排列。将这些与不同基序的存储几何结构进行比较。它的速度和效率使其成为结构基因组学项目的一个有益工具,特别是当蛋白质的生化功能尚未被表征时。