2fx6: Difference between revisions

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[[Image:2fx6.gif|left|200px]]
{{Seed}}
[[Image:2fx6.png|left|200px]]


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{{STRUCTURE_2fx6|  PDB=2fx6  |  SCENE=  }}  
{{STRUCTURE_2fx6|  PDB=2fx6  |  SCENE=  }}  


'''bovine trypsin complexed with 2-aminobenzamidazole'''
===bovine trypsin complexed with 2-aminobenzamidazole===




==Overview==
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Improved peptide-based inhibitors of human beta tryptase were discovered using information gleaned from tripeptide library screening and structure-guided design methods, including fragment screening. Our efforts sought to improve this class of inhibitors by replacing the traditional Lys or Arg P1 element. The optimized compounds display low nanomolar potency against the mast cell target and several hundred-fold selectivity with respect to serine protease off targets. Thus, replacement of Lys/Arg at P1 in a peptide-like scaffold does not need to be accompanied by a loss in target affinity.
The line below this paragraph, {{ABSTRACT_PUBMED_16681368}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16681368 is the PubMed ID number.
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{{ABSTRACT_PUBMED_16681368}}


==About this Structure==
==About this Structure==
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[[Category: S1 site]]
[[Category: S1 site]]
[[Category: Serine protease]]
[[Category: Serine protease]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May  4 04:24:32 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 23:06:35 2008''
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