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6wpv

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(New page: '''Unreleased structure''' The entry 6wpv is ON HOLD until Paper Publication Authors: Rosengren, K.J., Payne, C.D. Description: Solution NMR structure of the orbitide xanthoxycyclin D ...)
Current revision (11:06, 14 June 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 6wpv is ON HOLD until Paper Publication
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==Solution NMR structure of the orbitide xanthoxycyclin D==
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<StructureSection load='6wpv' size='340' side='right'caption='[[6wpv]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[6wpv]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Melicope_xanthoxyloides Melicope xanthoxyloides]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6WPV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6WPV FirstGlance]. <br>
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</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=6wpv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6wpv OCA], [https://pdbe.org/6wpv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6wpv RCSB], [https://www.ebi.ac.uk/pdbsum/6wpv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6wpv ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Cyclic peptides are reported to have antibacterial, antifungal and other bioactivities. Orbitides are a class of cyclic peptide that are small, head-to-tail cyclized, composed of proteinogenic amino acids, and lack disulfide bonds; they are also known in several genera of the plant family Rutaceae. Melicope xanthoxyloides is the Australian rain forest tree of the Rutaceae family in which evolidine - the first plant cyclic peptide - was discovered. Evolidine (cyclo-SFLPVNL) has subsequently been all but forgotten in the academic literature, so to redress this we used tandem mass spectrometry and de novo transcriptomics to rediscover evolidine and decipher its biosynthetic origin from a short precursor just 48 residues in length. We also identify another six M. xanthoxyloides orbitides using the same techniques. These peptides have atypically diverse C-termini consisting of residues not recognized by either of the known proteases plants use to macrocyclize peptides, suggesting new cyclizing enzymes await discovery. We examined the structure of two of the novel orbitides by NMR, finding one had a definable structure, whereas the other did not. Mining RNA-seq and whole genome sequencing data from other species of the Rutaceae family revealed a large and diverse family of peptides is encoded by similar sequences across the family and demonstrates how powerful de novo transcriptomics can be at accelerating the discovery of new peptide families.
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Authors: Rosengren, K.J., Payne, C.D.
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The genetic origin of evolidine, the first cyclopeptide discovered in plants, and related orbitides.,Fisher MF, Payne CD, Chetty T, Crayn DM, Berkowitz O, Whelan J, Rosengren KJ, Mylne JS J Biol Chem. 2020 Aug 19. pii: RA120.014781. doi: 10.1074/jbc.RA120.014781. PMID:32817170<ref>PMID:32817170</ref>
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Description: Solution NMR structure of the orbitide xanthoxycyclin D
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Payne, C.D]]
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<div class="pdbe-citations 6wpv" style="background-color:#fffaf0;"></div>
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[[Category: Rosengren, K.J]]
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Melicope xanthoxyloides]]
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[[Category: Payne CD]]
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[[Category: Rosengren KJ]]

Current revision

Solution NMR structure of the orbitide xanthoxycyclin D

PDB ID 6wpv

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