Ignoring a proteins sequence, say I have a predicted contact map plotted from a useful tool like ConKit, it can be quite easy to determine general regions of secondary structural features and if is running paralell or anti-paralell etc etc..

However besides this, does anybody have any good tips for breaking the predicted contact map down further to see regions which could be contacts involving loops or helices-loop contacts? In essence I am seeking some tips for how someone would step-by-step analyse different factors from a predicted contact map.

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