Maybe....

Nat 
Protoc.<http://www.ncbi.nlm.nih.gov/pubmed?term=Predicting%20protein-protein%20interactions%20on%20a%20proteome%20scale%20by%20matching%20evolutionary%20and%20structural%20similarities%20at%20interfaces%20using%20PRISM#>
 2011 Aug 11;6(9):1341-54. doi: 10.1038/nprot.2011.367.
Predicting protein-protein interactions on a proteome scale by matching 
evolutionary and structuralsimilarities at interfaces using PRISM.
Tuncbag 
N<http://www.ncbi.nlm.nih.gov/pubmed?term=Tuncbag%20N%5BAuthor%5D&cauthor=true&cauthor_uid=21886100>,
 Gursoy 
A<http://www.ncbi.nlm.nih.gov/pubmed?term=Gursoy%20A%5BAuthor%5D&cauthor=true&cauthor_uid=21886100>,
 Nussinov 
R<http://www.ncbi.nlm.nih.gov/pubmed?term=Nussinov%20R%5BAuthor%5D&cauthor=true&cauthor_uid=21886100>,
 Keskin 
O<http://www.ncbi.nlm.nih.gov/pubmed?term=Keskin%20O%5BAuthor%5D&cauthor=true&cauthor_uid=21886100>.
Source
Center for Computational Biology and Bioinformatics, College of Engineering, 
Koc University, Rumelifeneri Yolu, Sariyer Istanbul, Turkey.
Abstract
Prediction of protein-protein interactions at the structural level on the 
proteome scale is important because it allows prediction of protein function, 
helps drug discovery and takes steps toward genome-wide structural systems 
biology. We provide a protocol (termed PRISM, protein interactions bystructural 
matching) for large-scale prediction of protein-protein interactions and 
assembly of protein complex structures. The method consists of two components: 
rigid-body structural comparisons of target proteins to known template 
protein-protein interfaces and flexible refinement using a docking energy 
function. The PRISM rationale follows our observation that globally different 
protein structures can interact via similar architectural motifs.PRISM predicts 
binding residues by using structural similarity and evolutionary conservation 
of putative binding residue 'hot spots'. Ultimately,PRISM could help to 
construct cellular pathways and functional, proteome-scale annotation. PRISM is 
implemented in Python and runs in a UNIX environment. The program accepts 
Protein Data Bank-formatted protein structures and is available at 
http://prism.ccbb.ku.edu.tr/prism_protocol/.


On 8 Aug 2012, at 07:33, Careina Edgooms wrote:

Dear ccp4ers

I just wonder whether anybody knows if the PISA software could be used/modified 
to detect potential interfaces of interaction of different proteins? This would 
be very useful as a tool to validate protein-protein interactions detected by 
in vivo methods such as yeast 2 hybrid screens. If PISA is not quite there yet, 
does anyone know of other software that could do a similar thing?

Best
Careina

Roberto Steiner
Randall Division of Cell and Molecular Biophysics
King's College London

Room 3.10A
New Hunt's House
Guy's Campus
SE1 1UL, London, UK
Tel 0044-20-78488216
Fax 0044-20-78486435
[email protected]<mailto:[email protected]>




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