2f3x

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[[Image:2f3x.gif|left|200px]]
[[Image:2f3x.gif|left|200px]]
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{{Structure
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|PDB= 2f3x |SIZE=350|CAPTION= <scene name='initialview01'>2f3x</scene>, resolution 3.100&Aring;
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The line below this paragraph, containing "STRUCTURE_2f3x", 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=MLC:MALONYL-COENZYME+A'>MLC</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=
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or leave the SCENE parameter empty for the default display.
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|GENE= fapR ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1423 Bacillus subtilis])
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|DOMAIN=
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{{STRUCTURE_2f3x| PDB=2f3x | SCENE= }}
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|RELATEDENTRY=[[2f41|2F41]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2f3x FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2f3x OCA], [http://www.ebi.ac.uk/pdbsum/2f3x PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2f3x RCSB]</span>
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}}
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'''Crystal structure of FapR (in complex with effector)- a global regulator of fatty acid biosynthesis in B. subtilis'''
'''Crystal structure of FapR (in complex with effector)- a global regulator of fatty acid biosynthesis in B. subtilis'''
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[[Category: Buschiazzo, A.]]
[[Category: Buschiazzo, A.]]
[[Category: Guerin, M E.]]
[[Category: Guerin, M E.]]
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[[Category: hot-dog fold / malonyl-coa complex]]
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[[Category: Hot-dog fold / malonyl-coa complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 03:25:57 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:57:37 2008''
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Revision as of 00:25, 4 May 2008

Template:STRUCTURE 2f3x

Crystal structure of FapR (in complex with effector)- a global regulator of fatty acid biosynthesis in B. subtilis


Overview

Malonyl-CoA is an essential intermediate in fatty acid synthesis in all living cells. Here we demonstrate a new role for this molecule as a global regulator of lipid homeostasis in Gram-positive bacteria. Using in vitro transcription and binding studies, we demonstrate that malonyl-CoA is a direct and specific inducer of Bacillus subtilis FapR, a conserved transcriptional repressor that regulates the expression of several genes involved in bacterial fatty acid and phospholipid synthesis. The crystal structure of the effector-binding domain of FapR reveals a homodimeric protein with a thioesterase-like 'hot-dog' fold. Binding of malonyl-CoA promotes a disorder-to-order transition, which transforms an open ligand-binding groove into a long tunnel occupied by the effector molecule in the complex. This ligand-induced modification propagates to the helix-turn-helix motifs, impairing their productive association for DNA binding. Structure-based mutations that disrupt the FapR-malonyl-CoA interaction prevent DNA-binding regulation and result in a lethal phenotype in B. subtilis, suggesting this homeostatic signaling pathway as a promising target for novel chemotherapeutic agents against Gram-positive pathogens.

About this Structure

2F3X is a Single protein structure of sequence from Bacillus subtilis. Full crystallographic information is available from OCA.

Reference

Structural basis of lipid biosynthesis regulation in Gram-positive bacteria., Schujman GE, Guerin M, Buschiazzo A, Schaeffer F, Llarrull LI, Reh G, Vila AJ, Alzari PM, de Mendoza D, EMBO J. 2006 Sep 6;25(17):4074-83. Epub 2006 Aug 24. PMID:16932747 Page seeded by OCA on Sun May 4 03:25:57 2008

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