6kbc

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Current revision (10:29, 22 November 2023) (edit) (undo)
 
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<StructureSection load='6kbc' size='340' side='right'caption='[[6kbc]], [[Resolution|resolution]] 1.99&Aring;' scene=''>
<StructureSection load='6kbc' size='340' side='right'caption='[[6kbc]], [[Resolution|resolution]] 1.99&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[6kbc]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Chagb Chagb]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6KBC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6KBC FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6kbc]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Chaetomium_globosum_CBS_148.51 Chaetomium globosum CBS 148.51]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6KBC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6KBC 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=WK1:(2S)-3-[(2S,4E)-4-[[(1R,2S,4aR,6S,8R,8aS)-2-[(E)-but-2-en-2-yl]-6,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-oxidanyl-methylidene]-3,5-bis(oxidanylidene)pyrrolidin-2-yl]-2-methyl-2-oxidanyl-propanoic+acid'>WK1</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]] 1.99&#8491;</td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CHGG_02368 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=306901 CHAGB])</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=WK1:(2S)-3-[(2S,4E)-4-[[(1R,2S,4aR,6S,8R,8aS)-2-[(E)-but-2-en-2-yl]-6,8-dimethyl-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-oxidanyl-methylidene]-3,5-bis(oxidanylidene)pyrrolidin-2-yl]-2-methyl-2-oxidanyl-propanoic+acid'>WK1</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=6kbc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6kbc OCA], [https://pdbe.org/6kbc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6kbc RCSB], [https://www.ebi.ac.uk/pdbsum/6kbc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6kbc 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=6kbc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6kbc OCA], [https://pdbe.org/6kbc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6kbc RCSB], [https://www.ebi.ac.uk/pdbsum/6kbc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6kbc ProSAT]</span></td></tr>
</table>
</table>
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== Function ==
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[https://www.uniprot.org/uniprot/CGHA_CHAGB CGHA_CHAGB] Diels-Alderase; part of the gene cluster that mediates the biosynthesis of the tetramic acid Sch210972, a potential anti-HIV fungal natural product that contains a decalin core (PubMed:26360642). The PKS module of cghG together with the enoylreductase cghC catalyze the formation of the polyketide unit which is then conjugated to 4-hydroxyl-4-methyl glutamate (HMG) by the condensation domain of the cghG NRPS module (PubMed:26360642). One unique structural feature of Sch210972 is the tetramic acid motif proposed to be derived from the non-proteinogenic amino acid HMG, by a Dieckmann-type condensation catalyzed by the reductase domain of cghG (PubMed:26360642). The aldolase cghB catalyzes the aldol condensation of 2 molecules of pyruvic acid to yield the intermediate 4-hydroxyl-4-methyl-2-oxoglutarate (HMOG), which can then be stereoselectively transaminated by an unidentified enzyme to form HMG (PubMed:26360642). The Diels-Alderase cghA then uses the Dieckmann product released by cghG as substrate and catalyzes the Diels-Alder cycloaddition to form the decalin ring of Sch210972 (PubMed:26360642). CghA also suppresses the nonenzymatic formation of the alternative stereoisomer (PubMed:26360642).<ref>PMID:26360642</ref>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Chagb]]
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[[Category: Chaetomium globosum CBS 148 51]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Hara, K]]
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[[Category: Hara K]]
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[[Category: Hashimoto, H]]
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[[Category: Hashimoto H]]
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[[Category: Maeda, N]]
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[[Category: Maeda N]]
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[[Category: Sato, M]]
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[[Category: Sato M]]
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[[Category: Watanabe, K]]
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[[Category: Watanabe K]]
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[[Category: Diels-alderase]]
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[[Category: Unknown function]]
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Current revision

Crystal structure of CghA with Sch210972

PDB ID 6kbc

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