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3sju

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Current revision (09:51, 1 March 2024) (edit) (undo)
 
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<StructureSection load='3sju' size='340' side='right'caption='[[3sju]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
<StructureSection load='3sju' size='340' side='right'caption='[[3sju]], [[Resolution|resolution]] 2.40&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[3sju]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/As_4.1417 As 4.1417]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SJU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3SJU FirstGlance]. <br>
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<table><tr><td colspan='2'>[[3sju]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Streptomyces_griseoruber Streptomyces griseoruber]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SJU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3SJU FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</scene></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">X-ray diffraction, [[Resolution|Resolution]] 2.4&#8491;</td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">hedA ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1943 AS 4.1417])</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NDP:NADPH+DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE+PHOSPHATE'>NDP</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=3sju FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3sju OCA], [https://pdbe.org/3sju PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3sju RCSB], [https://www.ebi.ac.uk/pdbsum/3sju PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3sju ProSAT]</span></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=3sju FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3sju OCA], [https://pdbe.org/3sju PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3sju RCSB], [https://www.ebi.ac.uk/pdbsum/3sju PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3sju ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Function ==
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== Publication Abstract from PubMed ==
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[https://www.uniprot.org/uniprot/Q67G28_9ACTN Q67G28_9ACTN]
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Bacterial aromatic polyketides that include many antibiotic and antitumor therapeutics are biosynthesized by the type II polyketide synthase (PKS), which consists of 5-10 stand-alone enzymatic domains. Hedamycin, an antitumor antibiotic polyketide, is uniquely primed with a hexadienyl group generated by a type I PKS followed by coupling to a downstream type II PKS to biosynthesize a 24-carbon polyketide, whose C9 position is reduced by hedamycin type II ketoreductase (hedKR). HedKR is homologous to the actinorhodin KR (actKR), for which we have conducted extensive structural studies previously. How hedKR can accommodate a longer polyketide substrate than the actKR, and the molecular basis of its regio- and stereospecificities, is not well understood. Here we present a detailed study of hedKR that sheds light on its specificity. Sequence alignment of KRs predicts that hedKR is less active than actKR, with significant differences in substrate/inhibitor recognition. In vitro and in vivo assays of hedKR confirmed this hypothesis. The hedKR crystal structure further provides the molecular basis for the observed differences between hedKR and actKR in the recognition of substrates and inhibitors. Instead of the 94-PGG-96 motif observed in actKR, hedKR has the 92-NGG-94 motif, leading to S-dominant stereospecificity, whose molecular basis can be explained by the crystal structure. Together with mutations, assay results, docking simulations, and the hedKR crystal structure, a model for the observed regio- and stereospecificities is presented herein that elucidates how different type II KRs recognize substrates with different chain lengths, yet precisely reduce only the C9-carbonyl group. The molecular features of hedKR important for regio- and stereospecificities can potentially be applied to biosynthesize new polyketides via protein engineering that rationally controls polyketide ketoreduction.
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Structural and Biochemical Studies of the Hedamycin Type II Polyketide Ketoreductase (HedKR): Molecular Basis of Stereo- and Regiospecificities.,Javidpour P, Das A, Khosla C, Tsai SC Biochemistry. 2011 Aug 30;50(34):7426-39. Epub 2011 Aug 8. PMID:21776967<ref>PMID:21776967</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 3sju" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: As 4 1417]]
 
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Javidpour, P]]
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[[Category: Streptomyces griseoruber]]
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[[Category: Tsai, S C]]
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[[Category: Javidpour P]]
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[[Category: Oxidoreductase]]
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[[Category: Tsai S-C]]
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[[Category: Reductase]]
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[[Category: Rossmann fold]]
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[[Category: Short-chain dehydrogenase]]
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[[Category: Type ii polyketide ketoreductase]]
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Current revision

Hedamycin Polyketide Ketoreductase bound to NADPH

PDB ID 3sju

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