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| | ==Solution structure of Amphibian tachykinin Uperolein bound to DPC micelles== | | ==Solution structure of Amphibian tachykinin Uperolein bound to DPC micelles== |
| - | <StructureSection load='2gfr' size='340' side='right' caption='[[2gfr]], [[NMR_Ensembles_of_Models | 20 NMR models]]' scene=''> | + | <StructureSection load='2gfr' size='340' side='right'caption='[[2gfr]]' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[2gfr]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GFR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2GFR FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[2gfr]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Uperoleia_rugosa Uperoleia rugosa]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GFR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2GFR FirstGlance]. <br> |
| - | </td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=PCA:PYROGLUTAMIC+ACID'>PCA</scene></td></tr> | + | </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='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2gfr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2gfr OCA], [http://pdbe.org/2gfr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2gfr RCSB], [http://www.ebi.ac.uk/pdbsum/2gfr PDBsum]</span></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PCA:PYROGLUTAMIC+ACID'>PCA</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=2gfr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2gfr OCA], [https://pdbe.org/2gfr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2gfr RCSB], [https://www.ebi.ac.uk/pdbsum/2gfr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2gfr ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/TKN1_UPERU TKN1_UPERU]] Tachykinins are active peptides which excite neurons, evoke behavioral responses, are potent vasodilators and secretagogues, and contract (directly or indirectly) many smooth muscles. | + | [https://www.uniprot.org/uniprot/TKN1_UPERU TKN1_UPERU] Tachykinins are active peptides which excite neurons, evoke behavioral responses, are potent vasodilators and secretagogues, and contract (directly or indirectly) many smooth muscles. |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Cowsik, S M]] | + | [[Category: Large Structures]] |
| - | [[Category: Dike, A]] | + | [[Category: Uperoleia rugosa]] |
| - | [[Category: 3-10 helix]] | + | [[Category: Cowsik SM]] |
| - | [[Category: Dpc micelle]] | + | [[Category: Dike A]] |
| - | [[Category: Helix]]
| + | |
| - | [[Category: Lipid induced conformation]]
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| - | [[Category: Neuropeptide]]
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| Structural highlights
Function
TKN1_UPERU Tachykinins are active peptides which excite neurons, evoke behavioral responses, are potent vasodilators and secretagogues, and contract (directly or indirectly) many smooth muscles.
Publication Abstract from PubMed
Uperolein, a physalaemin-like endecapeptide, has been shown to be selective for Neurokinin 1 receptor. As a first step towards understanding the structure-activity relationship, we report the membrane-induced structure of Uperolein with the aid of circular dichroism and 2D (1)H NMR spectroscopy. Sequence-specific resonance assignments of protons have been made using correlation spectroscopy (TOCSY, DQF-COSY) and NOESY spectroscopy. The interproton distance constraints and dihedral angle constraints have been utilized to generate a family of structures using torsion angle molecular dynamics within program DYANA. The conformational range of the peptide revealed by NMR and CD studies has been analysed in terms of characteristic secondary features. Analysis of NMR data indicates that the global fold of Uperolein can be explained in terms of equilibrium between 3(10)-helix and alpha-helix from residues 5 to 11. An extended highly flexible N-terminus displays some degree of order and a possible turn structure. A comparison between the structures of Uperolein and Substance P, a prototype and endogenous Neurokinin 1 receptor agonist, indicates several common features in the distribution of hydrophobic and hydrophilic residues. Both the peptides show an amphiphilic character towards the middle region. The similarities suggest that the molecules interact with the receptor in an analogous manner.
Solution structure of amphibian tachykinin Uperolein bound to DPC micelles.,Dike A, Cowsik SM J Struct Biol. 2006 Dec;156(3):442-52. Epub 2006 Aug 1. PMID:16979908[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Dike A, Cowsik SM. Solution structure of amphibian tachykinin Uperolein bound to DPC micelles. J Struct Biol. 2006 Dec;156(3):442-52. Epub 2006 Aug 1. PMID:16979908 doi:http://dx.doi.org/S1047-8477(06)00211-5
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