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[[Image:1kj0.jpg|left|200px]]


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==SOLUTION STRUCTURE OF THE SMALL SERINE PROTEASE INHIBITOR SGTI==
The line below this paragraph, containing "STRUCTURE_1kj0", creates the "Structure Box" on the page.
<StructureSection load='1kj0' size='340' side='right'caption='[[1kj0]]' scene=''>
You may change the PDB parameter (which sets the PDB file loaded into the applet)
== Structural highlights ==
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
<table><tr><td colspan='2'>[[1kj0]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Schistocerca_gregaria Schistocerca gregaria]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1KJ0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1KJ0 FirstGlance]. <br>
or leave the SCENE parameter empty for the default display.
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 10 models</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1kj0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1kj0 OCA], [https://pdbe.org/1kj0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1kj0 RCSB], [https://www.ebi.ac.uk/pdbsum/1kj0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1kj0 ProSAT]</span></td></tr>
{{STRUCTURE_1kj0|  PDB=1kj0  |  SCENE= }}
</table>
 
== Function ==
'''SOLUTION STRUCTURE OF THE SMALL SERINE PROTEASE INHIBITOR SGTI'''
[https://www.uniprot.org/uniprot/SGP1_SCHGR SGP1_SCHGR] In vitro, SGPI-1/SGCI is active against alpha-chymotrypsin and trypsin while SGPI-2/SGTI is active against alpha-chymotrypsin and pancreatic elastase.
 
<div style="background-color:#fffaf0;">
 
== Publication Abstract from PubMed ==
==Overview==
The solution structure of three small serine proteinase inhibitors, two natural and one engineered protein, SGCI (Schistocerca gregaria chymotrypsin inhibitor), SGCI[L30R, K31M] and SGTI (Schistocerca gregaria trypsin inhibitor), were determined by homonuclear NMR-spectroscopy. The molecules exhibit different specificities towards target proteinases, where SGCI is a good chymotrypsin inhibitor, its mutant is a potent trypsin inhibitor, and SGTI inhibits both proteinases weakly. Interestingly, SGTI is a much better inhibitor of insect proteinases than of the mammalian ones used in common assays. All three molecules have a similar fold composed from three antiparallel beta-pleated sheets with three disulfide bridges. The proteinase binding loop has a somewhat distinct geometry in all three peptides. Moreover, the stabilization of the structure is different in SGCI and SGTI. Proton-deuterium exchange experiments are indicative of a highly rigid core in SGTI but not in SGCI. We suggest that the observed structural properties play a significant role in the specificity of these inhibitors.
The solution structure of three small serine proteinase inhibitors, two natural and one engineered protein, SGCI (Schistocerca gregaria chymotrypsin inhibitor), SGCI[L30R, K31M] and SGTI (Schistocerca gregaria trypsin inhibitor), were determined by homonuclear NMR-spectroscopy. The molecules exhibit different specificities towards target proteinases, where SGCI is a good chymotrypsin inhibitor, its mutant is a potent trypsin inhibitor, and SGTI inhibits both proteinases weakly. Interestingly, SGTI is a much better inhibitor of insect proteinases than of the mammalian ones used in common assays. All three molecules have a similar fold composed from three antiparallel beta-pleated sheets with three disulfide bridges. The proteinase binding loop has a somewhat distinct geometry in all three peptides. Moreover, the stabilization of the structure is different in SGCI and SGTI. Proton-deuterium exchange experiments are indicative of a highly rigid core in SGTI but not in SGCI. We suggest that the observed structural properties play a significant role in the specificity of these inhibitors.


==About this Structure==
Comparative structure analysis of proteinase inhibitors from the desert locust, Schistocerca gregaria.,Gaspari Z, Patthy A, Graf L, Perczel A Eur J Biochem. 2002 Jan;269(2):527-37. PMID:11856311<ref>PMID:11856311</ref>
1KJ0 is a [[Single protein]] structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1KJ0 OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
Comparative structure analysis of proteinase inhibitors from the desert locust, Schistocerca gregaria., Gaspari Z, Patthy A, Graf L, Perczel A, Eur J Biochem. 2002 Jan;269(2):527-37. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11856311 11856311]
</div>
[[Category: Single protein]]
<div class="pdbe-citations 1kj0" style="background-color:#fffaf0;"></div>
[[Category: Gaspari, Z.]]
== References ==
[[Category: Graf, L.]]
<references/>
[[Category: Patthy, A.]]
__TOC__
[[Category: Perczel, A.]]
</StructureSection>
[[Category: Inhibitor specificity]]
[[Category: Large Structures]]
[[Category: Serine protease inhibition]]
[[Category: Schistocerca gregaria]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May  2 22:48:14 2008''
[[Category: Gaspari Z]]
[[Category: Graf L]]
[[Category: Patthy A]]
[[Category: Perczel A]]

Latest revision as of 06:54, 30 October 2024

SOLUTION STRUCTURE OF THE SMALL SERINE PROTEASE INHIBITOR SGTI

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