Hi all:

I am working on a small (60a.a) archaeal protein. Scenario is:

  • Deletion strain shows better growth under low Fe conditions than the wild type strain.
  • At the same time more siderophores (Fe-chelators) are being produced in deletion strain under same low Fe condition. Seems a little contradictory to me.
  • Also, how can we predict protein function (if structure is known)?

    What approaches can I take?

    Thanks.

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