I would like to expand on the question and answer below and compare your experiences: Looking for ligands in many different soaks / cocrystals of your protein of interest, you still should do molecular replacement and a bit of refinement. I agree with Steve, but how much refinement is necessary and enough?
We have a specific case with a 24 kDa protein crystallizing in P6522 with resolution of 2.5 - 3 A, which should be comparable to most cases. The ligands have 10 - 20 non-hydrogen atoms (most of the time we don't know, we are actually screening for them). How far should we refine to see if we have only water molecules or a ligand bound - to an Rfree of 0.45 or 0.40 or 0.35? greetings Gottfried Dear all, Is there a simple way to determine whether ligand is bound or not by comparing the diffraction patterns between ligand-free (structure known) and ligand-soaked protein crystals? I would like to solve the ligand bound protein structure, but before I do so, I have to find out if the ligand is actually bound. Thank you very much! Best, Joe Having done this a few hundred times, I would strongly suggest that you just collect the data and solve the structure. Since you already have the apo structure solved, then it really isn't that much work to do an MR solution on the complex. Be aware that quite frequently there is enough non-isomorphism to necessitate partial refinement of the "complex" structure before recognizable density will appear for the ligand. The definitive answer can only be obtained with a full data set, so go for it. Good luck- Steve =================================================================== WEB-Mailer der Uni-Greifswald ( http://www.uni-greifswald.de/ ) ===================================================================
