We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

1t9e

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /><applet load="1t9e" size="450" color="white" frame="true" align="right" spinBox="true" caption="1t9e" /> '''NMR solution structure of a disulfide analog...)
Current revision (22:14, 26 March 2025) (edit) (undo)
 
(15 intermediate revisions not shown.)
Line 1: Line 1:
-
[[Image:1t9e.gif|left|200px]]<br /><applet load="1t9e" size="450" color="white" frame="true" align="right" spinBox="true"
 
-
caption="1t9e" />
 
-
'''NMR solution structure of a disulfide analogue of the cyclic sunflower trypsin inhibitor SFTI-1'''<br />
 
-
==Overview==
+
==NMR solution structure of a disulfide analogue of the cyclic sunflower trypsin inhibitor SFTI-1==
-
SFTI-1 is a novel 14 amino acid peptide comprised of a circular backbone, constrained by three proline residues, a hydrogen-bond network, and a, single disulfide bond. It is the smallest and most potent known, Bowman-Birk trypsin inhibitor and the only one with a cyclic peptidic, backbone. The solution structure of [ABA(3,11)]SFTI-1, a, disulfide-deficient analogue of SFTI-1, has been determined by (1)H NMR, spectroscopy. The lowest energy structures of native SFTI-1 and, [ABA(3,11)]SFTI-1 are similar and superimpose with a root-mean-square, deviation over the backbone and heavy atoms of 0.26 +/- 0.09 and 1.10 +/-, 0.22 A, respectively. The disulfide bridge in SFTI-1 was found to be a, minor determinant for the overall structure, but its removal resulted in a, slightly weakened hydrogen-bonding network. To further investigate the, role of the disulfide bridge, NMR chemical shifts for the backbone, H(alpha) protons of two disulfide-deficient linear analogues of SFTI-1, [ABA(3,11)]SFTI-1[6,5] and [ABA(3,11)]SFTI-1[1,14] were measured. These, correspond to analogues of the cleavage product of SFTI-1 and a putative, biosynthetic precursor, respectively. In contrast with the cyclic peptide, it was found that the disulfide bridge is essential for maintaining the, structure of these open-chain analogues. Overall, the hydrogen-bond, network appears to be a crucial determinant of the structure of SFTI-1, analogues.
+
<StructureSection load='1t9e' size='340' side='right'caption='[[1t9e]]' scene=''>
 +
== Structural highlights ==
 +
<table><tr><td colspan='2'>[[1t9e]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Helianthus_annuus Helianthus annuus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1T9E OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1T9E FirstGlance]. <br>
 +
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 20 models</td></tr>
 +
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ABA:ALPHA-AMINOBUTYRIC+ACID'>ABA</scene></td></tr>
 +
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1t9e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1t9e OCA], [https://pdbe.org/1t9e PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1t9e RCSB], [https://www.ebi.ac.uk/pdbsum/1t9e PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1t9e ProSAT]</span></td></tr>
 +
</table>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/SFTI1_HELAN SFTI1_HELAN] Inhibits trypsin, cathepsin G, elastase, chymotrypsin and thrombin. Does not inhibit factor Xa.<ref>PMID:10390350</ref>
 +
<div style="background-color:#fffaf0;">
 +
== Publication Abstract from PubMed ==
 +
SFTI-1 is a novel 14 amino acid peptide comprised of a circular backbone constrained by three proline residues, a hydrogen-bond network, and a single disulfide bond. It is the smallest and most potent known Bowman-Birk trypsin inhibitor and the only one with a cyclic peptidic backbone. The solution structure of [ABA(3,11)]SFTI-1, a disulfide-deficient analogue of SFTI-1, has been determined by (1)H NMR spectroscopy. The lowest energy structures of native SFTI-1 and [ABA(3,11)]SFTI-1 are similar and superimpose with a root-mean-square deviation over the backbone and heavy atoms of 0.26 +/- 0.09 and 1.10 +/- 0.22 A, respectively. The disulfide bridge in SFTI-1 was found to be a minor determinant for the overall structure, but its removal resulted in a slightly weakened hydrogen-bonding network. To further investigate the role of the disulfide bridge, NMR chemical shifts for the backbone H(alpha) protons of two disulfide-deficient linear analogues of SFTI-1, [ABA(3,11)]SFTI-1[6,5] and [ABA(3,11)]SFTI-1[1,14] were measured. These correspond to analogues of the cleavage product of SFTI-1 and a putative biosynthetic precursor, respectively. In contrast with the cyclic peptide, it was found that the disulfide bridge is essential for maintaining the structure of these open-chain analogues. Overall, the hydrogen-bond network appears to be a crucial determinant of the structure of SFTI-1 analogues.
-
==About this Structure==
+
Disulfide bond mutagenesis and the structure and function of the head-to-tail macrocyclic trypsin inhibitor SFTI-1.,Korsinczky ML, Clark RJ, Craik DJ Biochemistry. 2005 Feb 1;44(4):1145-53. PMID:15667208<ref>PMID:15667208</ref>
-
1T9E is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1T9E OCA].
+
-
==Reference==
+
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
-
Disulfide bond mutagenesis and the structure and function of the head-to-tail macrocyclic trypsin inhibitor SFTI-1., Korsinczky ML, Clark RJ, Craik DJ, Biochemistry. 2005 Feb 1;44(4):1145-53. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15667208 15667208]
+
</div>
-
[[Category: Single protein]]
+
<div class="pdbe-citations 1t9e" style="background-color:#fffaf0;"></div>
-
[[Category: Clark, R.J.]]
+
-
[[Category: Craik, D.J.]]
+
-
[[Category: Korsinczky, M.L.J.]]
+
-
[[Category: disulfide mutant]]
+
-
[[Category: nmr]]
+
-
[[Category: sunflower trypsin inhibitor]]
+
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 01:53:17 2007''
+
==See Also==
 +
*[[Trypsin inhibitor 3D structures|Trypsin inhibitor 3D structures]]
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Helianthus annuus]]
 +
[[Category: Large Structures]]
 +
[[Category: Clark RJ]]
 +
[[Category: Craik DJ]]
 +
[[Category: Korsinczky MLJ]]

Current revision

NMR solution structure of a disulfide analogue of the cyclic sunflower trypsin inhibitor SFTI-1

PDB ID 1t9e

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools