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位点引擎:结合位点与蛋白质-蛋白质相互作用界面的识别和比较。

SiteEngines: recognition and comparison of binding sites and protein-protein interfaces.

作者信息

Shulman-Peleg Alexandra, Nussinov Ruth, Wolfson Haim J

机构信息

School of Computer Science, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 69978, Israel.

出版信息

Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W337-41. doi: 10.1093/nar/gki482.

DOI:10.1093/nar/gki482
PMID:15980484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1160242/
Abstract

Protein surface regions with similar physicochemical properties and shapes may perform similar functions and bind similar binding partners. Here we present two web servers and software packages for recognition of the similarity of binding sites and interfaces. Both methods recognize local geometrical and physicochemical similarity, which can be present even in the absence of overall sequence or fold similarity. The first method, SiteEngine (http:/bioinfo3d.cs.tau.ac.il/SiteEngine), receives as an input two protein structures and searches the complete surface of one protein for regions similar to the binding site of the other. The second, Interface-to-Interface (I2I)-SiteEngine (http:/bioinfo3d.cs.tau.ac.il/I2I-SiteEngine), compares protein-protein interfaces, which are regions of interaction between two protein molecules. It receives as an input two structures of protein-protein complexes, extracts the interfaces and finds the three-dimensional transformation that maximizes the similarity between two pairs of interacting binding sites. The output of both servers consists of a superimposition in PDB file format and a list of physicochemical properties shared by the compared entities. The methods are highly efficient and the freely available software packages are suitable for large-scale database searches of the entire PDB.

摘要

具有相似物理化学性质和形状的蛋白质表面区域可能执行相似的功能并结合相似的结合伴侣。在此,我们展示了两个用于识别结合位点和界面相似性的网络服务器和软件包。这两种方法都能识别局部几何和物理化学相似性,即使在整体序列或折叠相似性不存在的情况下也可能存在这种相似性。第一种方法是SiteEngine(http:/bioinfo3d.cs.tau.ac.il/SiteEngine),它以两个蛋白质结构作为输入,并在一个蛋白质的整个表面搜索与另一个蛋白质的结合位点相似的区域。第二种方法是界面到界面(I2I)-SiteEngine(http:/bioinfo3d.cs.tau.ac.il/I2I-SiteEngine),它比较蛋白质-蛋白质界面,即两个蛋白质分子之间的相互作用区域。它以两个蛋白质-蛋白质复合物的结构作为输入,提取界面并找到使两对相互作用的结合位点之间的相似性最大化的三维变换。两个服务器的输出都包括PDB文件格式的叠加以及被比较实体共享的物理化学性质列表。这些方法效率很高,免费提供的软件包适用于对整个PDB进行大规模数据库搜索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3313/1160242/9210e2daabca/gki482f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3313/1160242/9210e2daabca/gki482f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3313/1160242/9210e2daabca/gki482f1.jpg

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