Karplus and Diederichs. Science 2012.

Hendrickson. Science. 2012


some references :-)

2015-01-16 16:01 GMT+01:00 Almudena Ponce Salvatierra <maps.fa...@gmail.com>
:

> Dear Izuok,
>
> 1. There are different metrics you can look at in order to know on how
> much anomalous signal you can rely: CCano, ΔFano/σΔF, and ΔFano/F, In the
> CCP4 study weekend in Nottingham last weekend, Prof. Janet Smith said that
> for them it was the last one, ΔFano/F, the one working better as an
> overall estimate of the anomalous signal. Otherwise, you can look at the
> XDS output and see where the CCano drops below 0.3, or where the SigAno
> drops below 1... that should give you an idea. Otherwise put your mtz
> through Phenix Xtriage, it will output a good analysis of the data as well
> as reccommend a resolution cutoff for anomalous resolution.
>
> 2. I don't really know... well if you are working with a protein, there
> might be sites (Cys residues) where Hg would be more likely to be found...
> But I am not sure here... I would use as a first guess same number of sites
> as of Cys residues... but I am not working with proteins so I'm just
> guessing... probably there is a better way.
>
> All the best,
>
> Almudena
>
> 2015-01-16 15:33 GMT+01:00 luzuok <luzuo...@126.com>:
>
>>
>> Dear all,
>>     I'm doing Hg SAD phasing for the first time, and I met some problem:
>> 1. How to assess the anomalous signal after I process the data and get my
>> mtz file?
>>     My labmate doesn't scan the fluorescence signal. Actually, I don't
>> quite understand why we use fluorescence to detect anomalous signal.
>> 2. How to estimate the number of heave atom in one unit cell? by soaking
>> heavy atom derivatives.
>>
>> Best!
>>
>> Lu Zuokun
>> Nankai University
>>
>> --
>> 卢作焜
>> 南开大学新生物站A202
>>
>>
>>
>
>
> --
> Almudena Ponce-Salvatierra
> Macromolecular crystallography and Nucleic acid chemistry
> Max Planck Institute for Biophysical Chemistry
> Am Fassberg 11 37077 Göttingen
> Germany
>
>


-- 
Almudena Ponce-Salvatierra
Macromolecular crystallography and Nucleic acid chemistry
Max Planck Institute for Biophysical Chemistry
Am Fassberg 11 37077 Göttingen
Germany

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