5od1
From Proteopedia
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==Structure of the engineered metalloesterase MID1sc10 complexed with a phosphonate transition state analogue== | ==Structure of the engineered metalloesterase MID1sc10 complexed with a phosphonate transition state analogue== | ||
| - | <StructureSection load='5od1' size='340' side='right' caption='[[5od1]], [[Resolution|resolution]] 1.34Å' scene=''> | + | <StructureSection load='5od1' size='340' side='right'caption='[[5od1]], [[Resolution|resolution]] 1.34Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[5od1]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Synthetic_construct_sequences Synthetic construct sequences]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5OD1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5OD1 FirstGlance]. <br> | <table><tr><td colspan='2'>[[5od1]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Synthetic_construct_sequences Synthetic construct sequences]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5OD1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5OD1 FirstGlance]. <br> | ||
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<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=5od1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5od1 OCA], [http://pdbe.org/5od1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5od1 RCSB], [http://www.ebi.ac.uk/pdbsum/5od1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5od1 ProSAT]</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=5od1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5od1 OCA], [http://pdbe.org/5od1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5od1 RCSB], [http://www.ebi.ac.uk/pdbsum/5od1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5od1 ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | Primordial sequence signatures in modern proteins imply ancestral origins tracing back to simple peptides. Although short peptides seldom adopt unique folds, metal ions might have templated their assembly into higher-order structures in early evolution and imparted useful chemical reactivity. Recapitulating such a biogenetic scenario, we have combined design and laboratory evolution to transform a zinc-binding peptide into a globular enzyme capable of accelerating ester cleavage with exacting enantiospecificity and high catalytic efficiency (k cat/K M ~ 10(6) M(-1) s(-1)). The simultaneous optimization of structure and function in a naive peptide scaffold not only illustrates a plausible enzyme evolutionary pathway from the distant past to the present but also proffers exciting future opportunities for enzyme design and engineering. | ||
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| + | Evolution of a highly active and enantiospecific metalloenzyme from short peptides.,Studer S, Hansen DA, Pianowski ZL, Mittl PRE, Debon A, Guffy SL, Der BS, Kuhlman B, Hilvert D Science. 2018 Dec 14;362(6420):1285-1288. doi: 10.1126/science.aau3744. PMID:30545884<ref>PMID:30545884</ref> | ||
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| + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
| + | </div> | ||
| + | <div class="pdbe-citations 5od1" style="background-color:#fffaf0;"></div> | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Large Structures]] | ||
[[Category: Synthetic construct sequences]] | [[Category: Synthetic construct sequences]] | ||
[[Category: Hansen, D A]] | [[Category: Hansen, D A]] | ||
Revision as of 06:29, 29 May 2019
Structure of the engineered metalloesterase MID1sc10 complexed with a phosphonate transition state analogue
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