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

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edited by richtesn
on 2021/06/14 11:45

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To version 8.1

edited by richtesn
on 2021/06/14 11:46

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@@ -16,7 +16,7 @@
  == Input Data ==
--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|.
++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]]
  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.