View source for 5wva


==Serratia marcescens short-chain dehydrogenase/reductase F98Y/F202Y mutant==
<StructureSection load='5wva' size='340' side='right'caption='[[5wva]], [[Resolution|resolution]] 1.47&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[5wva]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WVA OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=5WVA FirstGlance]. <br>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5wul|5wul]], [[5wuw|5wuw]]</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=5wva FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wva OCA], [http://pdbe.org/5wva PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5wva RCSB], [http://www.ebi.ac.uk/pdbsum/5wva PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5wva ProSAT]</span></td></tr>
</table>
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== Publication Abstract from PubMed ==
Bioconversion is useful to produce optically pure enantiomers in the pharmaceutical industry, thereby avoiding problems with side reactions during organic synthesis processes. A short-chain dehydrogenase/reductase from Serratia marcescens BCRC 10948 (SmSDR) can stereoselectively convert 1-(3-hydroxyphenyl)-2-(methylamino) ethanone (HPMAE) into (R)-phenylephrine [(R)-PE], which is marketed medically as a nasal decongestant agent. The whole-cell conversion process for the synthesis of (R)-PE using SmSDR was reported to have an unexpectedly low conversion rate. We reported the crystal structure of the SmSDR and designed profitable variants to improve the enzymatic activity by structure-guided approach. Several important residues in the structure were observed to form hydrophobic clusters that stabilize the mobile loops surrounding the pocket. Of these, Phe98 and Phe202 face toward each other and connect the upper curvature from the two arms (i.e., the alpha7 helix and loopbeta4-alpha4). The mutant structure of the double substitutions (F98YF202Y) exhibited a hydrogen bond between the curvatures that stabilizes the flexible arms. Site-directed mutagenesis characterization revealed that the mutations (F98Y, F98YF202Y, and F98YF202L) of the flexible loops that stabilize the region exhibited a higher transformation activity toward HPMAE. Together, our results suggest a robust structure-guided approach that can be used to generate a valuable engineered variant for pharmaceutical applications.

Structure-guided design of Serratia marcescens short-chain dehydrogenase/reductase for stereoselective synthesis of (R)-phenylephrine.,Liu JS, Kuan YC, Tsou Y, Lin TY, Hsu WH, Yang MT, Lin JY, Wang WC Sci Rep. 2018 Feb 2;8(1):2316. doi: 10.1038/s41598-018-19235-y. PMID:29396495<ref>PMID:29396495</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Large Structures]]
[[Category: Liu, J S]]
[[Category: Tsou, Y]]
[[Category: Wang, W C]]
[[Category: F98y/f202y mutant]]
[[Category: Oxidoreductase]]
[[Category: Serratia marcescen]]
[[Category: Short-chain dehydrogenase/reductase]]