Thanks all for information and tips.

With the help, I did some quick'n dirty analysis



Total PDB (2011-01-11)                                                          
            70303

Method Xray                                                                     
                    61092

HHHHH                                                                           
                          10060

Method Xray and HHHHH                                                           
      9098



TEV-recognition

HHHHHX{0,30}ENLYFQ                                                              
         918

Method Xray and HHHHHX{0,30}ENLYFQ                                   877

Method Xray and ENLYFQ X{0,30} HHHHH                                 26



EK recognition

HHHHHX{0,30}DDDDK                                                               
         126

Method Xray and HHHHHX{0,30}DDDDK                                    117

DDDKX{0,30}HHHHH                                                                
           14

Method Xray and DDDKX{0,30}HHHHH                                       14



Thrombin

HHHHHX{0,30}LVPRGS                                                              
         1519

Method XRAY and HHHHHX{0,30}LVPRGS                                 1400

LVPRGSX{0,30}HHHHH                                                              
         37

XRAY and LVPRGSX{0,30}HHHHH                                                  35



3C

HHHHHX{0,30}LE[VAT]LFQGP                                                        
 42

XRAY and HHHHHX{0,30}LE[VAT]LFQGP                                     40

LE[VAT]LFQGPX{0,30}HHHHH                                                        
 1

XRAY and LE[VAT]LFQGPX{0,30}HHHHH                                     1



Xa

HHHHHX{0,30}I[ED]GR                                                             
          89

XRAY and HHHHHX{0,30}I[ED]GR                                                  75

I[ED]GRX{0,30}HHHHH                                                             
          41

XRAY and I[ED]GRX{0,30}HHHHH                                                  36



XRAY and not any of the above patterns                                   6477



>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>

Actually, typically we set up crystal trials for both cleaved and uncleaved 
protein right away at the same time (if there's enough protein and the cleavage 
works).
Cheers
phx
>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>



On 07/01/2011 15:10, Bosch, Juergen wrote:

I vaguely remember a paper by Aled Edwards, where they did the statistics for 
their targets at SGC. As far as I recall they engineer with cleavable tag 
purify and cyrstallize it first with tag and only if they don't get crystals or 
a structure they cleave off the tag and rerun the screens. I think the numbers 
where 30% of the proteins have been cleaved.



Jürgen

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>



"Carson, M. et al. (2007). His-tag impact on structure. Acta Crystallographica 
Section D 63, 295-301".

A contribution I made to a thread on the CCP4 emails (I can give you a link to 
the archive if you want to find it and don't) was:
"As at 2 January 2006 there were 236 structures with at least one chain
containing 5 or more consecutive Histidine residues. Atom records were
used in order to extract out the sequences of the polypeptides.
.....
Erdahl Teber

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>



Reference from Wladek Minor (Kirillova, Acta Cryst D63, 2007, 348-354), this 
structure shows an ordered 10 residue segment from an uncleaved tag including 
TEV recognition site.



>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>



Dear Arjan,



Try the Hampton Research website (www.hamptonresearch.com). They have done 
surveys of the crystallization  community about his-tag on or off and the 
results should still be there.



Good luck.

Bryan

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>



Hi Arjan -



Since sequence searches of the PDB use the SEQRES records (which are supposed 
to represent the crystallization construct) rather than the deposited 
coordinates, you should be able to craft a Blast search with tight enough 
restraints that searching for 'HHHHHH' or some of the most common protease 
sites will give you a useful answer.  Using NCBI's Blast page, and searching 
the PDB for an 8-His sequence, I got 205 hits (but there were probably more, 
and I hit some sort of cap).



Hope that helps,

Matt

>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>



The RCSB PDB site (www.pdb.org) provides as sequence motif search as an 
advanced search option. For example to search for a N-terminal (His)6 tag, use 
the following regular expression:



^HHHHHH



or HHHHHH to find any sequence with a (His)6 pattern.



Click on this link to retrieve all sequences with a (His)6 pattern:

http://www.pdb.org/pdb/search/smart.do?smartSearchSubtype_0=MotifQuery&motif_0=HHHHHH



For more details about the sequence motif search are available at:

http://www.pdb.org/pdb/staticHelp.do?p=help/advancedsearch/sequenceMotif.html



Best regards,



Peter Rose

RCSB PDB










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