-161-275-5090/5658
> Fax: +44-161-275-1505
> email: [EMAIL PROTECTED]
> Intranet:http://www.intranet.ls,manchester.ac.uk/facilities/research/xraycrystallography
> Internet:http://www.ls.manchester.ac.uk/research/facilities/xray
>
>
--
Peng Zhang, Ph.D. Student
Institute of Bi
real native one(2.7A),it seems OK with R=0.24 and Rf=0.28.
Does anyone have the similar experience?
what should I pay attention to when using the sad/mad data as the native
one for modelling and refinement?
Thanks in advance.
--
Peng Zhang, Ph.D. Student
Institute of Biochemistry and Cell
e Free R set from the native to the Se data?
> Eleanor
>
>
> Peng Zhang wrote:
>> Dear friends,
>>
>> Recently, I have solved a structure using mad method. When using the
>> peak
>> data(2.3A) as the native for structure refinement, the gap between R
>&g
a and peak data.I try to compare them because I want to make it clear
that the difference may be caused by the mad data while not the model
itself.
Thanks.
> Hi Peng Zhang,
>
> The presence of radiation damage might cause some problems.
> Do so see any obvious features in the difference ma
data sets - then run uniqueify -f FreeRflag merged.mtz
>
> That will keep the existing flags and generate new ones for the new
> reflections..
>
> Then if you want to you can convert back to the CNS format.
> Eleanor
>
>
> Peng Zhang wrote:
>> Hi, Peter,
>>
>
data sets - then run uniqueify -f FreeRflag merged.mtz
>
> That will keep the existing flags and generate new ones for the new
> reflections..
>
> Then if you want to you can convert back to the CNS format.
> Eleanor
>
>
> Peng Zhang wrote:
>> Hi, Peter,
>>
>
OAQ OAR OAS OAQ
torsion T022 0 O4* C1* N9 C4 C8 N7 C5 C4 N3 C2 \
N1 C6 N6
--
Peng Zhang, Ph.D. Student
Institute of Biochemistry and Cell Biology
Shanghai Institutes for Biological Sciences
Chinese Academy of Sciences
320 Yue-Yang Road
Shanghai
