2fs8: Difference between revisions

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|PDB= 2fs8 |SIZE=350|CAPTION= <scene name='initialview01'>2fs8</scene>, resolution 2.500&Aring;
|PDB= 2fs8 |SIZE=350|CAPTION= <scene name='initialview01'>2fs8</scene>, resolution 2.500&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=C3A:ALLYL {(1S)-1-[(5-{4-[(2,3-DIHYDRO-1H-INDEN-2-YLAMINO)CARBONYL]BENZYL}-1,2,4-OXADIAZOL-3-YL)CARBONYL]-3-PYRROLIDIN-3-YLPROPYL}CARBAMATE'>C3A</scene>
|LIGAND= <scene name='pdbligand=C3A:ALLYL+{(1S)-1-[(5-{4-[(2,3-DIHYDRO-1H-INDEN-2-YLAMINO)CARBONYL]BENZYL}-1,2,4-OXADIAZOL-3-YL)CARBONYL]-3-PYRROLIDIN-3-YLPROPYL}CARBAMATE'>C3A</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/Tryptase Tryptase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.59 3.4.21.59]  
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Tryptase Tryptase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.59 3.4.21.59] </span>
|GENE= TPSB2, TPS2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= TPSB2, TPS2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=[[2fs9|2FS9]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2fs8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2fs8 OCA], [http://www.ebi.ac.uk/pdbsum/2fs8 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2fs8 RCSB]</span>
}}
}}


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[[Category: Tryptase]]
[[Category: Tryptase]]
[[Category: Somoza, J R.]]
[[Category: Somoza, J R.]]
[[Category: C3A]]
[[Category: 29382]]
[[Category: 29382]]
[[Category: proteinase]]
[[Category: proteinase]]
[[Category: serine protease]]
[[Category: serine protease]]


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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:06:59 2008''

Revision as of 00:07, 31 March 2008

File:2fs8.gif


Drag the structure with the mouse to rotate
2fs8, resolution 2.500Å
Ligands: C3A
Gene: TPSB2, TPS2 (Homo sapiens)
Activity: Tryptase, with EC number 3.4.21.59
Related: 2FS9


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



Human beta-tryptase II with inhibitor CRA-29382


Overview

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.

About this Structure

2FS8 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

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