Changes for page 2.2 Identify potential protein binding sites by comparing the electrostatic potentials of a set of protein isoforms
Last modified by richtesn on 2023/06/14 12:18
Summary
-
Page properties (1 modified, 0 added, 0 removed)
Details
- Page properties
-
- Content
-
... ... @@ -12,11 +12,11 @@ 12 12 13 13 ~* For details on computation of the electrostatic potential see [[Calculate electrostatic potential>>doc:Collabs.computation-of-protein-association-rates.d.WebHome]]. 14 14 15 -~* For details on the similarity computations and pipsa algorithm ,see:ref:`el_multipipsa`15 +~* For details on the similarity computations and [[pipsa algorithm>>doc:Collabs.computation-of-protein-association-rates.Compare a specific region of the electrostatic potentials surrounding a set of protein isoforms with multipipsa.WebHome]]. 16 16 17 17 == Input Data == 18 18 19 -In this use case, we use as our input structure a structure of the catalytic domain of the enzyme adenylyl cyclase 5 (AC5), modelled during the work described in |doi_tong|.19 +In this use case, we use as our input structure a structure of the catalytic domain of the enzyme adenylyl cyclase 5 (AC5), modelled during the work described in [[Tong et al. (2016)>>https://doi.org/10.1002/prot.25167]] 20 20 21 21 The structures of the AC isoforms were created via homology modelling using the same template. The region where there are significant structural differences between the isoforms is in a flexible loop region that was not defined in the template structure. There are also variations in sequence length across AC isoforms in this region. 22 22 ... ... @@ -41,7 +41,7 @@ 41 41 42 42 == Related Jupyter Notebook == 43 43 44 -Please note: Fortechnical reasonsthe notebookscurrently are not running liveinthecollaboratory.44 +Please note: In the lab where the notebook is running, please select the kernel: EBRAINS-23.02 45 45 46 46 {{jupyterlink}} 47 47 https://lab.ebrains.eu/user-redirect/lab/tree/shared/Molecular%20Tools:%20protein%20association%20rates%20and%20binding%20sites/JN/Identify_potential_protein_binding_sites_of_a_set_of_protein_isoforms.ipynb