1999
DOI: 10.1002/(sici)1097-0134(19990801)36:2<192::aid-prot5>3.3.co;2-c
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Probing the modelled structure of Wheatwin1 by controlled proteolysis and sequence analysis of unfractionated digestion mixtures

Abstract: We set up a method to get rapid information on the three-dimensional structure of peptide and proteins of known sequence. Both native and alkylated polypeptide is hydrolyzed with a number of proteases at different digestion times and the resulting mixtures are compared by HPLC analysis to establish the differences in the hydrolysis pathways of the folded and unfolded molecule. Then, the unfractionated digestion mixtures of the native polypeptide are submitted to automatic sequence analysis to identify the hydr… Show more

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Cited by 2 publications
(2 citation statements)
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“…The 3D model of DQ2 was created following the homology modelling procedure [16][17][18][19] already used with success by our group [20][21][22][23][24]. In brief, searches for sequence similarity within databases were performed with the BLAST program [25].…”
Section: Protein Modellingmentioning
confidence: 99%
“…The 3D model of DQ2 was created following the homology modelling procedure [16][17][18][19] already used with success by our group [20][21][22][23][24]. In brief, searches for sequence similarity within databases were performed with the BLAST program [25].…”
Section: Protein Modellingmentioning
confidence: 99%
“…Most of the peptide bonds hydrolyzed by trypsin are located in regions without secondary-structure elements such as helices or b-strands, which may confer protease resistance on the backbone [36][37][38][39].…”
Section: Hplcmentioning
confidence: 99%