2l22

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Current revision (06:51, 1 May 2024) (edit) (undo)
 
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== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[2l22]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Pseudomonas_fluorescens Pseudomonas fluorescens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L22 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2L22 FirstGlance]. <br>
<table><tr><td colspan='2'>[[2l22]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Pseudomonas_fluorescens Pseudomonas fluorescens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L22 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2L22 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=2l22 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l22 OCA], [https://pdbe.org/2l22 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2l22 RCSB], [https://www.ebi.ac.uk/pdbsum/2l22 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2l22 ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2l22 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l22 OCA], [https://pdbe.org/2l22 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2l22 RCSB], [https://www.ebi.ac.uk/pdbsum/2l22 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2l22 ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
[https://www.uniprot.org/uniprot/Q8RL76_PSEFL Q8RL76_PSEFL]
[https://www.uniprot.org/uniprot/Q8RL76_PSEFL Q8RL76_PSEFL]
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<div style="background-color:#fffaf0;">
 
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== Publication Abstract from PubMed ==
 
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Type I polyketide synthases often use programmed beta-branching, via enzymes of a 'hydroxymethylglutaryl-CoA synthase (HCS) cassette', to incorporate various side chains at the second carbon from the terminal carboxylic acid of growing polyketide backbones. We identified a strong sequence motif in acyl carrier proteins (ACPs) where beta-branching is known to occur. Substituting ACPs confirmed a correlation of ACP type with beta-branching specificity. Although these ACPs often occur in tandem, NMR analysis of tandem beta-branching ACPs indicated no ACP-ACP synergistic effects and revealed that the conserved sequence motif forms an internal core rather than an exposed patch. Modeling and mutagenesis identified ACP helix III as a probable anchor point of the ACP-HCS complex whose position is determined by the core. Mutating the core affects ACP functionality, whereas ACP-HCS interface substitutions modulate system specificity. Our method for predicting beta-carbon branching expands the potential for engineering new polyketides and lays a basis for determining specificity rules.
 
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A conserved motif flags acyl carrier proteins for beta-branching in polyketide synthesis.,Haines AS, Dong X, Song Z, Farmer R, Williams C, Hothersall J, Ploskon E, Wattana-Amorn P, Stephens ER, Yamada E, Gurney R, Takebayashi Y, Masschelein J, Cox RJ, Lavigne R, Willis CL, Simpson TJ, Crosby J, Winn PJ, Thomas CM, Crump MP Nat Chem Biol. 2013 Sep 22. doi: 10.1038/nchembio.1342. PMID:24056399<ref>PMID:24056399</ref>
 
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
 
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</div>
 
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<div class="pdbe-citations 2l22" style="background-color:#fffaf0;"></div>
 
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== References ==
 
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<references/>
 
__TOC__
__TOC__
</StructureSection>
</StructureSection>

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Mupirocin didomain ACP

PDB ID 2l22

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