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Re: [ccp4bb] Data collection of SAD (MAD) data of Copper-containing protein |
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CCP4bb navigationCCP4bb <-- 2007 <-- March 2007 <-- 15 March 2007Subject: Re: Data collection of SAD (MAD) data of Copper-containing protein From: ES manian1 {- at -} VSNL {- dot -} COM Date: 2007-03-15 Is the resolution of the data sufficient to apply direct methods to find only the copper atoms, then use the copper atom positions in an old-fashioned 'heavy-atom' phasing method, combined with direct methods? Incidentally, was the following publication of any relevance in your efforts? Acta Crystallogr D Biol Crystallogr. 1998 Jul 1;54(Pt 4):629-35. Structure determination of a 16.8 kDa copper protein at 2.1 A resolution using anomalous scattering data with direct methods. Harvey I, Hao Q, Duke EM, Ingledew WJ, Hasnain SS. ES University of Madras Yi Xue wrote: >Dear all: > We already got nice crystals of a drug-protein complex, however, MR >failed due to the huge copies (>12) of protein molecules per asu. Protein >itself is a small one, only ~70 aa. > Later on, we collected MAD data of copper (copper : protein ~ 1: 1), >Rsym of the data was around ~9%, the anomalous signals were weak, and only >good to ~6A, the data also failed to solve the phases. > Thus, basically, the Cu anomallous signal is very weak, and the >crystals are kind of sensitive to radiation, it is dying but not that fast. > I am wondering, Do we stand any chances to solve the phases by Cu MAD >or SAD? > > >Any suggestions or comments are highly appreciated? >Yi > > > CCP4bb navigationCCP4bb <-- 2007 <-- March 2007 <-- 15 March 2007 |
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