1x9e

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[[Image:1x9e.jpg|left|200px]]
[[Image:1x9e.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 1x9e |SIZE=350|CAPTION= <scene name='initialview01'>1x9e</scene>, resolution 2.40&Aring;
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The line below this paragraph, containing "STRUCTURE_1x9e", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Hydroxymethylglutaryl-CoA_synthase Hydroxymethylglutaryl-CoA synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.10 2.3.3.10] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE= MVAS ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1351 Enterococcus faecalis])
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-->
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|DOMAIN=
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{{STRUCTURE_1x9e| PDB=1x9e | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1x9e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1x9e OCA], [http://www.ebi.ac.uk/pdbsum/1x9e PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1x9e RCSB]</span>
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}}
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'''Crystal structure of HMG-CoA synthase from Enterococcus faecalis'''
'''Crystal structure of HMG-CoA synthase from Enterococcus faecalis'''
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[[Category: Sutherlin, A.]]
[[Category: Sutherlin, A.]]
[[Category: Vartia, A A.]]
[[Category: Vartia, A A.]]
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[[Category: thiolase family]]
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[[Category: Thiolase family]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 14:44:23 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:46:30 2008''
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Revision as of 11:44, 3 May 2008

Template:STRUCTURE 1x9e

Crystal structure of HMG-CoA synthase from Enterococcus faecalis


Overview

Biosynthesis of the isoprenoid precursor, isopentenyl diphosphate, is a critical function in all independently living organisms. There are two major pathways for this synthesis, the non-mevalonate pathway found in most eubacteria and the mevalonate pathway found in animal cells and a number of pathogenic bacteria. An early step in this pathway is the condensation of acetyl-CoA and acetoacetyl-CoA into HMG-CoA, catalyzed by the enzyme HMG-CoA synthase. To explore the possibility of a small molecule inhibitor of the enzyme functioning as a non-cell wall antibiotic, the structure of HMG-CoA synthase from Enterococcus faecalis (MVAS) was determined by selenomethionine MAD phasing to 2.4 A and the enzyme complexed with its second substrate, acetoacetyl-CoA, to 1.9 A. These structures show that HMG-CoA synthase from Enterococcus is a member of the family of thiolase fold enzymes and, while similar to the recently published HMG-CoA synthase structures from Staphylococcus aureus, exhibit significant differences in the structure of the C-terminal domain. The acetoacetyl-CoA binary structure demonstrates reduced coenzyme A and acetoacetate covalently bound to the active site cysteine through a thioester bond. This is consistent with the kinetics of the reaction that have shown acetoacetyl-CoA to be a potent inhibitor of the overall reaction, and provides a starting point in the search for a small molecule inhibitor.

About this Structure

1X9E is a Single protein structure of sequence from Enterococcus faecalis. Full crystallographic information is available from OCA.

Reference

X-ray crystal structures of HMG-CoA synthase from Enterococcus faecalis and a complex with its second substrate/inhibitor acetoacetyl-CoA., Steussy CN, Vartia AA, Burgner JW 2nd, Sutherlin A, Rodwell VW, Stauffacher CV, Biochemistry. 2005 Nov 1;44(43):14256-67. PMID:16245942 Page seeded by OCA on Sat May 3 14:44:23 2008

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