4a9w

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[[Image:4a9w.png|left|200px]]
 
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{{STRUCTURE_4a9w| PDB=4a9w | SCENE= }}
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==Flavin-containing monooxygenase from Stenotrophomonas maltophilia==
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<StructureSection load='4a9w' size='340' side='right'caption='[[4a9w]], [[Resolution|resolution]] 2.72&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4a9w]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Stenotrophomonas_maltophilia Stenotrophomonas maltophilia]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4A9W OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4A9W FirstGlance]. <br>
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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]] 2.72&#8491;</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=FAD:FLAVIN-ADENINE+DINUCLEOTIDE'>FAD</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></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=4a9w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4a9w OCA], [https://pdbe.org/4a9w PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4a9w RCSB], [https://www.ebi.ac.uk/pdbsum/4a9w PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4a9w ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/B2FRL2_STRMK B2FRL2_STRMK]
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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A gene from the marine bacterium Stenotrophomonas maltophilia encodes a 38.6 kDa FAD-containing flavoprotein (Uniprot B2FLR2) named S. maltophilia flavin-containing monooxygenase (SMFMO), which catalyses the oxidation of thioethers and also the regioselective Baeyer-Villiger oxidation of the model substrate bicyclo[3.2.0]hept-2-en-6-one. The enzyme was unusual in its ability to employ either NADH or NADPH as nicotinamide cofactor. The K(M) and k(cat) values for NADH were 23.7+/-9.1 muM and 0.029 s(-1) and 27.3+/-5.3 muM and 0.022 s(-1) for NADPH. However, k(cat) /K(M) value for the ketone substrate in the presence of 100 muM cofactor was 17 times greater for NADH than for NADPH. SMFMO catalysed the quantitative conversion of 5 mM ketone in the presence of substoichiometric concentrations of NADH with the formate dehydrogenase cofactor recycling system, to give the 2-oxa and 3-oxa lactone products of Baeyer-Villiger reaction in a ratio of 5:1, albeit with poor enantioselectivity. The conversion with NADPH was 15 %. SMFMO also catalysed the NADH-dependent transformation of prochiral aromatic thioethers, giving in the best case, 80 % ee for the transformation of p-chlorophenyl methyl sulfide to its R enantiomer. The structure of SMFMO reveals that the relaxation in cofactor specificity appears to be accomplished by the substitution of an arginine residue, responsible for recognition of the 2'-phosphate on the NADPH ribose in related NADPH-dependent FMOs, with a glutamine residue in SMFMO. SMFMO is thus representative of a separate class of single-component, flavoprotein monooxygenases that catalyse NADH-dependent oxidations from which possible sequences and strategies for developing NADH-dependent biocatalysts for asymmetric oxygenation reactions might be identified.
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===Flavin-containing monooxygenase from Stenotrophomonas maltophilia===
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A Flavoprotein Monooxygenase that Catalyses a Baeyer-Villiger Reaction and Thioether Oxidation Using NADH as the Nicotinamide Cofactor.,Jensen CN, Cartwright J, Ward J, Hart S, Turkenburg JP, Ali ST, Allen MJ, Grogan G Chembiochem. 2012 Apr 16;13(6):872-8. doi: 10.1002/cbic.201200006. Epub 2012 Mar , 13. PMID:22416037<ref>PMID:22416037</ref>
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{{ABSTRACT_PUBMED_22416037}}
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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 4a9w" style="background-color:#fffaf0;"></div>
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==About this Structure==
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==See Also==
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[[4a9w]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Stenotrophomonas_maltophilia Stenotrophomonas maltophilia]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4A9W OCA].
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*[[Monooxygenase 3D structures|Monooxygenase 3D structures]]
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== References ==
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==Reference==
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<references/>
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<ref group="xtra">PMID:022416037</ref><references group="xtra"/>
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__TOC__
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[[Category: Flavin-containing monooxygenase]]
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</StructureSection>
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[[Category: Large Structures]]
[[Category: Stenotrophomonas maltophilia]]
[[Category: Stenotrophomonas maltophilia]]
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[[Category: Ali, S T.]]
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[[Category: Ali ST]]
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[[Category: Allen, M J.]]
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[[Category: Allen MJ]]
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[[Category: Cartwright, J.]]
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[[Category: Cartwright J]]
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[[Category: Grogan, G.]]
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[[Category: Grogan G]]
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[[Category: Hart, S.]]
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[[Category: Hart S]]
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[[Category: Jensen, C N.]]
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[[Category: Jensen CN]]
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[[Category: Turkenburg, J P.]]
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[[Category: Turkenburg JP]]
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[[Category: Baeyer-villiger]]
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[[Category: Fad]]
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[[Category: Oxidoreductase]]
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Current revision

Flavin-containing monooxygenase from Stenotrophomonas maltophilia

PDB ID 4a9w

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