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| <StructureSection load='5j7x' size='340' side='right'caption='[[5j7x]], [[Resolution|resolution]] 1.90Å' scene=''> | | <StructureSection load='5j7x' size='340' side='right'caption='[[5j7x]], [[Resolution|resolution]] 1.90Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[5j7x]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Aspfl Aspfl]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5J7X OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5J7X FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[5j7x]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Aspergillus_flavus Aspergillus flavus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5J7X OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5J7X FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=TAM:TRIS(HYDROXYETHYL)AMINOMETHANE'>TAM</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9Å</td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">AFLA_016370 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5059 ASPFL])</td></tr>
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=TAM:TRIS(HYDROXYETHYL)AMINOMETHANE'>TAM</scene></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=5j7x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5j7x OCA], [http://pdbe.org/5j7x PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5j7x RCSB], [http://www.ebi.ac.uk/pdbsum/5j7x PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5j7x 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=5j7x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5j7x OCA], [https://pdbe.org/5j7x PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5j7x RCSB], [https://www.ebi.ac.uk/pdbsum/5j7x PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5j7x ProSAT]</span></td></tr> |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/B8N653_ASPFN B8N653_ASPFN] |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| __TOC__ | | __TOC__ |
| </StructureSection> | | </StructureSection> |
- | [[Category: Aspfl]] | + | [[Category: Aspergillus flavus]] |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Ferroni, F M]] | + | [[Category: Ferroni FM]] |
- | [[Category: Opperman, D J]] | + | [[Category: Opperman DJ]] |
- | [[Category: Smit, M S]] | + | [[Category: Smit MS]] |
- | [[Category: Tolmie, C]] | + | [[Category: Tolmie C]] |
- | [[Category: Baeyer-villiger monooxygenase]]
| + | |
- | [[Category: Oxidoreductase]]
| + | |
| Structural highlights
Function
B8N653_ASPFN
Publication Abstract from PubMed
Baeyer-Villiger monooxygenases (BVMOs) are biocatalysts that convert ketones to esters. Due to their high regio-, stereo- and enantioselectivity and ability to catalyse these reactions under mild conditions, they have gained interest as alternatives to chemical Baeyer-Villiger catalysts. Despite their widespread occurrence within the fungal kingdom, most of the currently characterized BVMOs are from bacterial origin. Here we report the catalytic and structural characterization of BVMOAFL838 from Aspergillus flavus. BVMOAFL838 converts linear and aryl ketones with high regioselectivity. Steady-state kinetics revealed BVMOAFL838 to show significant substrate inhibition with phenylacetone, which was more pronounced at low pH, enzyme and buffer concentrations. Para substitutions on the phenyl group significantly improved substrate affinity and increased turnover frequencies. Steady-state kinetics revealed BVMOAFL838 to preferentially oxidize aliphatic ketones and aryl ketones when the phenyl group are separated by at least two carbons from the carbonyl group. The X-ray crystal structure, the first of a fungal BVMO, was determined at 1.9 A and revealed the typical overall fold seen in type I bacterial BVMOs. The active site Arg and Asp are conserved, with the Arg found in the "in" position. Similar to phenylacetone monooxygenase (PAMO), a two residue insert relative to cyclohexanone monooxygenase (CHMO) forms a bulge within the active site. Approximately half of the "variable" loop is folded into a short alpha-helix and covers part of the active site entry channel in the non-NADPH bound structure. This study adds to the current efforts to rationalize the substrate scope of BVMOs through comparative catalytic and structural investigation of different BVMOs.
Structural and Catalytic Characterization of a Fungal Baeyer-Villiger Monooxygenase.,Ferroni FM, Tolmie C, Smit MS, Opperman DJ PLoS One. 2016 Jul 29;11(7):e0160186. doi: 10.1371/journal.pone.0160186., eCollection 2016. PMID:27472055[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Ferroni FM, Tolmie C, Smit MS, Opperman DJ. Structural and Catalytic Characterization of a Fungal Baeyer-Villiger Monooxygenase. PLoS One. 2016 Jul 29;11(7):e0160186. doi: 10.1371/journal.pone.0160186., eCollection 2016. PMID:27472055 doi:http://dx.doi.org/10.1371/journal.pone.0160186
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