7dro: Difference between revisions

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New page: '''Unreleased structure''' The entry 7dro is ON HOLD Authors: Description: Category: Unreleased Structures
 
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'''Unreleased structure'''


The entry 7dro is ON HOLD
==Structure of ATP-grasp ligase PsnB complexed with minimal precursor==
<StructureSection load='7dro' size='340' side='right'caption='[[7dro]], [[Resolution|resolution]] 3.25&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[7dro]] is a 10 chain structure with sequence from [https://en.wikipedia.org/wiki/Plesiocystis_pacifica_SIR-1 Plesiocystis pacifica SIR-1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7DRO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7DRO FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 3.25&#8491;</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=7dro FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7dro OCA], [https://pdbe.org/7dro PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7dro RCSB], [https://www.ebi.ac.uk/pdbsum/7dro PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7dro ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/A6G4D7_9DELT A6G4D7_9DELT]
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Graspetides, also known as omega-ester-containing peptides (OEPs), are a family of ribosomally synthesized and post-translationally modified peptides (RiPPs) bearing side chain-to-side chain macrolactone or macrolactam linkages. Here, we present the molecular details of precursor peptide recognition by the macrocyclase enzyme PsnB in the biosynthesis of plesiocin, a group 2 graspetide. Biochemical analysis revealed that, in contrast to other RiPPs, the core region of the plesiocin precursor peptide noticeably enhanced the enzyme-precursor interaction via the conserved glutamate residues. We obtained four crystal structures of symmetric or asymmetric PsnB dimers, including those with a bound core peptide and a nucleotide, and suggest that the highly conserved Arg213 at the enzyme active site specifically recognizes a ring-forming acidic residue before phosphorylation. Collectively, this study provides insights into the mechanism underlying substrate recognition in graspetide biosynthesis and lays a foundation for engineering new variants.


Authors:  
Molecular mechanism underlying substrate recognition of the peptide macrocyclase PsnB.,Song I, Kim Y, Yu J, Go SY, Lee HG, Song WJ, Kim S Nat Chem Biol. 2021 Nov;17(11):1123-1131. doi: 10.1038/s41589-021-00855-x. Epub , 2021 Sep 2. PMID:34475564<ref>PMID:34475564</ref>


Description:  
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
<div class="pdbe-citations 7dro" style="background-color:#fffaf0;"></div>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Plesiocystis pacifica SIR-1]]
[[Category: Kim S]]
[[Category: Song I]]
[[Category: Song W]]
[[Category: Yu J]]

Latest revision as of 16:38, 29 November 2023

Structure of ATP-grasp ligase PsnB complexed with minimal precursor

7dro, resolution 3.25Å

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