Changes for page MLCE - PPIs prediction
Last modified by emacasali on 2023/01/11 16:04
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... ... @@ -18,10 +18,32 @@ 18 18 19 19 Mathematically speaking this process is an energy decomposition method, which starts with the calculation of the unbound part of the potential E (van der Waals, electrostatic interactions, solvent effects) through an MM/GBSA calculation: 20 20 21 +(% style="text-align:center" %) 22 +[[image:image-20230111154750-1.png||height="263" width="536"]] 21 21 22 - =Whohas access?=24 +Since the first eigenvector contains most of the relevant energy information about the interactions in the system, we can approximate the matrix energy to the first eigenvector: 23 23 24 -Describe the audience of this collab. 26 +(% style="text-align:center" %) 27 +[[image:image-20230111154917-1.png||height="47" width="225"]] 28 + 29 +Finally, we can filter the approximated interaction matrix Mio for residues that are in geometric proximity in the structure (closer than 6Å): 30 + 31 +(% style="text-align:center" %) 32 +[[image:image-20230111155023-1.png||height="48" width="253"]] 33 + 34 + 35 += How to use the script = 36 + 37 +Please see the attached documentation files in Drive repository. 38 + 39 + 40 += References = 41 + 42 +~1. Scarbelli, G.; Morra, G.; Colombo, G., Predicting Interaction Sites from the Energetics of Isolated Proteins: A New Approach to Epitope Mapping, Biophys. J., 2010, 98, 1966, [[https:~~/~~/doi.org/10.1016%2Fj.bpj.2010.01.014>>https://doi.org/10.1016%2Fj.bpj.2010.01.014]] 43 + 44 +2. Genoni, A.; Morra, G.; Colombo, G., Identification of Domains in Protein Structures from the Analysis of Intramolecular Interactions, J. Phys. Chem. B, 2012, 116, 10, 3331–3343, [[https:~~/~~/doi.org/10.1021/jp210568a>>https://doi.org/10.1021/jp210568a]] 45 + 46 + 25 25 ))) 26 26 27 27 ... ... @@ -31,6 +31,7 @@ 31 31 {{toc/}} 32 32 {{/box}} 33 33 56 + 34 34 35 35 ))) 36 36 )))
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