4lcm: Difference between revisions

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==Simvastatin Synthase (LOVD), from Aspergillus Terreus, LovD9 mutant (simh9014)==
==Simvastatin Synthase (LOVD), from Aspergillus Terreus, LovD9 mutant (simh9014)==
<StructureSection load='4lcm' size='340' side='right' caption='[[4lcm]], [[Resolution|resolution]] 3.19&Aring;' scene=''>
<StructureSection load='4lcm' size='340' side='right' caption='[[4lcm]], [[Resolution|resolution]] 3.19&Aring;' scene=''>
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3hl9|3hl9]], [[3hlb|3hlb]], [[3hlc|3hlc]], [[3hld|3hld]], [[3hle|3hle]], [[3hlf|3hlf]], [[3hlg|3hlg]], [[4lcl|4lcl]]</td></tr>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[3hl9|3hl9]], [[3hlb|3hlb]], [[3hlc|3hlc]], [[3hld|3hld]], [[3hle|3hle]], [[3hlf|3hlf]], [[3hlg|3hlg]], [[4lcl|4lcl]]</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">lovD ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=33178 ASPTE])</td></tr>
<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">lovD ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=33178 ASPTE])</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4lcm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4lcm OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4lcm RCSB], [http://www.ebi.ac.uk/pdbsum/4lcm PDBsum]</span></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4lcm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4lcm OCA], [http://pdbe.org/4lcm PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4lcm RCSB], [http://www.ebi.ac.uk/pdbsum/4lcm PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4lcm ProSAT]</span></td></tr>
</table>
</table>
<div style="background-color:#fffaf0;">
<div style="background-color:#fffaf0;">
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
</div>
</div>
<div class="pdbe-citations 4lcm" style="background-color:#fffaf0;"></div>
==See Also==
*[[Simvastatin Synthase|Simvastatin Synthase]]
== References ==
== References ==
<references/>
<references/>

Revision as of 12:24, 11 August 2016

Simvastatin Synthase (LOVD), from Aspergillus Terreus, LovD9 mutant (simh9014)Simvastatin Synthase (LOVD), from Aspergillus Terreus, LovD9 mutant (simh9014)

Structural highlights

4lcm is a 4 chain structure with sequence from Aspte. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Gene:lovD (ASPTE)
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Publication Abstract from PubMed

Natural enzymes have evolved to perform their cellular functions under complex selective pressures, which often require their catalytic activities to be regulated by other proteins. We contrasted a natural enzyme, LovD, which acts on a protein-bound (LovF) acyl substrate, with a laboratory-generated variant that was transformed by directed evolution to accept instead a small free acyl thioester and no longer requires the acyl carrier protein. The resulting 29-mutant variant is 1,000-fold more efficient in the synthesis of the drug simvastatin than the wild-type LovD. This is to our knowledge the first nonpatent report of the enzyme currently used for the manufacture of simvastatin as well as the intermediate evolved variants. Crystal structures and microsecond-scale molecular dynamics simulations revealed the mechanism by which the laboratory-generated mutations free LovD from dependence on protein-protein interactions. Mutations markedly altered conformational dynamics of the catalytic residues, obviating the need for allosteric modulation by the acyl carrier LovF.

The role of distant mutations and allosteric regulation on LovD active site dynamics.,Jimenez-Oses G, Osuna S, Gao X, Sawaya MR, Gilson L, Collier SJ, Huisman GW, Yeates TO, Tang Y, Houk KN Nat Chem Biol. 2014 Jun;10(6):431-6. doi: 10.1038/nchembio.1503. Epub 2014 Apr, 13. PMID:24727900[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

See Also

References

  1. Jimenez-Oses G, Osuna S, Gao X, Sawaya MR, Gilson L, Collier SJ, Huisman GW, Yeates TO, Tang Y, Houk KN. The role of distant mutations and allosteric regulation on LovD active site dynamics. Nat Chem Biol. 2014 Jun;10(6):431-6. doi: 10.1038/nchembio.1503. Epub 2014 Apr, 13. PMID:24727900 doi:http://dx.doi.org/10.1038/nchembio.1503

4lcm, resolution 3.19Å

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