2hcp: Difference between revisions
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{{Theoretical_model}} | |||
==THREE-DIMENSIONAL MODEL OF GREENBUG ACETYLCHOLINESTERASE== | ==THREE-DIMENSIONAL MODEL OF GREENBUG ACETYLCHOLINESTERASE== | ||
<StructureSection load='2hcp' size='340' side='right' caption='[[2hcp]]' scene=''> | <StructureSection load='2hcp' size='340' side='right'caption='[[2hcp]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>For a <b>guided tour on the structure components</b> use [ | <table><tr><td colspan='2'>For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2HCP FirstGlance]. <br> | ||
</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | </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=2hcp FirstGlance], [https://www.ebi.ac.uk/pdbsum/2hcp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2hcp ProSAT]</span></td></tr> | ||
</table> | </table> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
<div class="pdbe-citations 2hcp" style="background-color:#fffaf0;"></div> | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Theoretical Model]] | |||
[[Category: Large Structures]] | |||
[[Category: Pang, Y P]] | [[Category: Pang, Y P]] | ||
Latest revision as of 14:07, 5 January 2022
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THREE-DIMENSIONAL MODEL OF GREENBUG ACETYLCHOLINESTERASETHREE-DIMENSIONAL MODEL OF GREENBUG ACETYLCHOLINESTERASE
Structural highlights
Publication Abstract from PubMedCurrent anticholinesterase pesticides developed during World War II are toxic to mammals because they target a catalytic serine residue of acetylcholinesterases (AChEs) in insects and in mammals. A sequence analysis of AChEs from 68 species and three-dimensional models of the greenbug and English grain aphid AChEs reported herein reveal that a cysteine residue is present at the active sites of greenbug and aphid AChEs but absent at those of mammalian AChEs. This discovery enables the design of novel and safe pesticides that target the cysteine residue rather than the ubiquitous serine residue. Species marker for developing novel and safe pesticides.,Pang YP Bioorg Med Chem Lett. 2007 Jan 1;17(1):197-9. Epub 2006 Oct 12. PMID:17046256[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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