Hello all, I have a 1.8A structure (Rfree/Rwork = 20.5/17.4) with 1420 water molecules modelled. There are approximately a dozen waters, all well structured with hydrogen bonds to protein atoms, with positive difference density (>4sigma, sometimes >5) at their centre. The only ions present in my buffer were Cs, Cl and a small amount of Na. I thought Cl ions might be a possibility, but many of them are in close proximity to acidic residues and/or one-another. It's probably worth noting that the same structure solved using data to 2.25A from the same crystal at a different wavelength doesn't contain these peaks (the offending waters look normal).
Has any come across this before? Thoughts? Thanks, Andrew Marshall PhD Candidate Laboratory of Protein Crystallography Dept. of Molecular and Cellular Biology School of Biological Sciences The University of Adelaide
