TY - JOUR
T1 - SiteEngines
T2 - Recognition and comparison of binding sites and protein-protein interfaces
AU - Shulman-Peleg, Alexandra
AU - Nussinov, Ruth
AU - Wolfson, Haim J.
N1 - Funding Information:
We would like to thank Dr Shuo Liang Lin for valuable suggestions. This research has been supported in part by the Center of Excellence in Geometric Computing and its Applications funded by the Israel Science Foundation (administered by the Israel Academy of Sciences) and by the Tel Aviv University Adams Brain Center. The research of H.J.W. is partially supported by the Hermann Minkowski-Minerva Center for Geometry at Tel Aviv University. The research of R.N. has been funded in whole or in part with Federal funds from the National Cancer Institute, National Institutes of Health, under contract number NO1-CO-12400. The content of this publication does not necessarily reflect the view or policies of the Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply endorsement by the U.S. Government. Funding to pay the Open Access publication charges for this article was provided by SAIC-Frederick, Inc.
PY - 2005/7
Y1 - 2005/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=23144456254&partnerID=8YFLogxK
U2 - 10.1093/nar/gki482
DO - 10.1093/nar/gki482
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C2 - 15980484
AN - SCOPUS:23144456254
SN - 0305-1048
VL - 33
SP - W337-W341
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - SUPPL. 2
ER -