Dear all, Firstly - many thanks to Kay Diederichs and Graeme Winter.
The “memory” error was in fact due to certain diffraction images having very few (weak), if any spots - essentially they were ‘blank’. By excluding these images, and with a combination of Xia2, plus XDS + Aimless, I was finally able to satisfactorily process the data. FYI: The resultant mtz extends to ~ 3.6 Angstrom, with a CC(1/2) of 0.633. Although the resolution isn’t the greatest, 8-fold NCS makes the resultant maps rather nice. A great many thanks to others who offered useful tips and advice. A slightly less tired Antony. - - - - - - - - - - - - - - - - - - Dr Antony W Oliver Senior Research Fellow CR-UK DNA Repair Enzymes Group Genome Damage and Stability Centre Science Park Road University of Sussex Falmer, Brighton, BN1 9RQ - - - - - - - - - - - - - - - - - - email: [email protected]<mailto:[email protected]> tel (office): +44 (0)1273 678349 tel (lab): +44 (0)1273 677512 http://www.sussex.ac.uk/lifesci/oliverlab http://tinyurl.com/aw-oliver - - - - - - - - - - - - - - - - - -
