Dear Madhurima, Small protein structures can be very difficult to solve by MR due to an unfavorable ratio between inter- and intra-molecular vectors in the pattersons. I am currently also struggling with some data sets myself.
However, there are things you could (and should) try: 1) If your search protein forms an oligomer, e.g. dimer, trimer etc., generate this oligomer and use this as a search model. Having a bigger search model will significantly increase your signal to noise ratio. 2) Try as many different MR programs as you can lay your hand on. Sometimes one succeeds, where others fail. I would at least try phaser. 3) Do not run the program(s) using the default parameters, but carefully read the manual and adjust the parameters based on the size and shape of your search protein. If your protein contains cysteines and/or methionines, you could look if there is any anomalous signal in your home source data. Getting higher resolution synchrotron data may not hurt as well. Good luck! Herman Von: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] Im Auftrag von Madhurima Roy Gesendet: Donnerstag, 9. Februar 2017 05:18 An: CCP4BB@JISCMAIL.AC.UK Betreff: [ccp4bb] Problem with MolRep Hi all, I have a small protein which is of 6 kDa including six histidine tag. The protein crystallized in the conditions given bellow : a) 0.1M Sodium acetate trihydrate pH 4.6, 3M NaCl. b) 0.1 M Bis-tris pH 5.5, 2M Ammonium sulphate. The crystals are plate shaped in both conditions.We collected diffraction data at our home source using Rigaku RaxisIV and processed the data using XDS. In spite of good homology, the protein structure cannot be solved by MolRep , the contrast is very low approx 1.65. The PDB Blast result is given below: 38.1(total score), 70%(query coverage) 1e-05 (E-value) and 50%(Identity) . The screen shot of the statistics showing R factor and quality of fit in CORRECT.LP file is enclosed below. Kindly help. Thanks in advance. Madhurima
