Changes for page Molecular Tools: protein association rates and binding sites
Last modified by richtesn on 2022/05/23 22:36
Summary
-
Page properties (2 modified, 0 added, 0 removed)
Details
- Page properties
-
- Author
-
... ... @@ -1,1 +1,1 @@ 1 -XWiki.ri chtesn1 +XWiki.dariak - Content
-
... ... @@ -4,8 +4,6 @@ 4 4 ((( 5 5 = Molecular Tools: protein association rates and binding sites = 6 6 7 -This collab contains a set of tools and tutorials for exploring protein binding properties based on their electrostatics and estimation of protein-protein association rates 8 - 9 9 Authors: Stefan Richter 10 10 ))) 11 11 ))) ... ... @@ -16,18 +16,8 @@ 16 16 ((( 17 17 = What can I find here? = 18 18 19 -Please note, the corresponding usecases as jupyter notebooks will be transferred from Collaboratory 1. So far they can be found here: 20 -[[https:~~/~~/collab.humanbrainproject.eu/#/collab/1655/nav/362934>>https://collab.humanbrainproject.eu/#/collab/1655/nav/362934]] 21 - 22 -The corresponding guidebooks can be found here: 23 -[[https:~~/~~/collab.humanbrainproject.eu/#/collab/1655/nav/18580>>https://collab.humanbrainproject.eu/#/collab/1655/nav/18580]] 24 - 25 -The descriptions of 26 - 27 27 * ((( 28 -Tools and tutorials that describes how to: 29 - 30 -* simulate protein-protein association using Brownian Dynamics (BD) simulations (web server webSDA) 18 +Tools and tutorials that describes how to:* simulate protein-protein association using Brownian Dynamics (BD) simulations (web server webSDA) 31 31 * analyse the results of a Brownian dynamics simulation for calculating protein-protein association rate constants 32 32 * compute protein electrostatic potential (under development) 33 33 * ((( ... ... @@ -34,7 +34,7 @@ 34 34 compare the electrostatic potentials surrounding a set of protein isoforms or specific regions with multipipsa (under development) 35 35 ))) 36 36 * ((( 37 -identify potential protein binding sites by comparing the electrostatic potentials of a set of protein isoforms (under development)25 +identify potential protein binding sites by comparing the electrostatic potentials of a set of protein isoforms 38 38 ))) 39 39 ))) 40 40