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2fpz

From Proteopedia

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[[Image:2fpz.gif|left|200px]]
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{{STRUCTURE_2fpz| PDB=2fpz | SCENE= }}
{{STRUCTURE_2fpz| PDB=2fpz | SCENE= }}
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'''Human tryptase with 2-amino benzimidazole'''
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===Human tryptase with 2-amino benzimidazole===
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==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.
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(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: Drug design]]
[[Category: Drug design]]
[[Category: Serine protease]]
[[Category: Serine protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 04:11:11 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 21:08:04 2008''

Revision as of 18:08, 27 July 2008

Image:2fpz.png

Template:STRUCTURE 2fpz

Human tryptase with 2-amino benzimidazole

Template:ABSTRACT PUBMED 16681368

About this Structure

2FPZ is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structure-guided design of peptide-based tryptase inhibitors., McGrath ME, Sprengeler PA, Hirschbein B, Somoza JR, Lehoux I, Janc JW, Gjerstad E, Graupe M, Estiarte A, Venkataramani C, Liu Y, Yee R, Ho JD, Green MJ, Lee CS, Liu L, Tai V, Spencer J, Sperandio D, Katz BA, Biochemistry. 2006 May 16;45(19):5964-73. PMID:16681368

Page seeded by OCA on Sun Jul 27 21:08:04 2008

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