2h3g: Difference between revisions

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New page: left|200px<br /><applet load="2h3g" size="350" color="white" frame="true" align="right" spinBox="true" caption="2h3g, resolution 2.000Å" /> '''Structure of the Ty...
 
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==Overview==
==Overview==
Coenzyme A (CoASH) is the major low-molecular weight thiol in, Staphylococcus aureus and a number of other bacteria; the crystal, structure of the S. aureus coenzyme A-disulfide reductase (CoADR), which, maintains the reduced intracellular state of CoASH, has recently been, reported [Mallett, T.C., Wallen, J.R., Karplus, P.A., Sakai, H., Tsukihara, T., and Claiborne, A. (2006) Biochemistry 45, 11278-89]. In, this report we demonstrate that CoASH is the major thiol in Bacillus, anthracis; a bioinformatics analysis indicates that three of the four, proteins responsible for the conversion of pantothenate (Pan) to CoASH in, Escherichia coli are conserved in B. anthracis. In contrast, a novel type, III pantothenate kinase (PanK) catalyzes the first committed step in the, biosynthetic pathway in B. anthracis; unlike the E. coli type I PanK, this, enzyme is not subject to feedback inhibition by CoASH. The crystal, structure of B. anthracis PanK (BaPanK), solved using multiwavelength, anomalous dispersion data and refined at a resolution of 2.0 A, demonstrates that BaPanK is a new member of the Acetate and Sugar, Kinase/Hsc70/Actin (ASKHA) superfamily. The Pan and ATP substrates have, been modeled into the active-site cleft; in addition to providing a clear, rationale for the absence of CoASH inhibition, analysis of the Pan-binding, pocket has led to the development of two new structure-based motifs (the, PAN and INTERFACE motifs). Our analyses also suggest that the type III, PanK in the spore-forming B. anthracis plays an essential role in the, novel thiol/disulfide redox biology of this category A biodefense, pathogen.
Coenzyme A (CoASH) is the major low-molecular weight thiol in Staphylococcus aureus and a number of other bacteria; the crystal structure of the S. aureus coenzyme A-disulfide reductase (CoADR), which maintains the reduced intracellular state of CoASH, has recently been reported [Mallett, T.C., Wallen, J.R., Karplus, P.A., Sakai, H., Tsukihara, T., and Claiborne, A. (2006) Biochemistry 45, 11278-89]. In this report we demonstrate that CoASH is the major thiol in Bacillus anthracis; a bioinformatics analysis indicates that three of the four proteins responsible for the conversion of pantothenate (Pan) to CoASH in Escherichia coli are conserved in B. anthracis. In contrast, a novel type III pantothenate kinase (PanK) catalyzes the first committed step in the biosynthetic pathway in B. anthracis; unlike the E. coli type I PanK, this enzyme is not subject to feedback inhibition by CoASH. The crystal structure of B. anthracis PanK (BaPanK), solved using multiwavelength anomalous dispersion data and refined at a resolution of 2.0 A, demonstrates that BaPanK is a new member of the Acetate and Sugar Kinase/Hsc70/Actin (ASKHA) superfamily. The Pan and ATP substrates have been modeled into the active-site cleft; in addition to providing a clear rationale for the absence of CoASH inhibition, analysis of the Pan-binding pocket has led to the development of two new structure-based motifs (the PAN and INTERFACE motifs). Our analyses also suggest that the type III PanK in the spore-forming B. anthracis plays an essential role in the novel thiol/disulfide redox biology of this category A biodefense pathogen.


==About this Structure==
==About this Structure==
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==Reference==
==Reference==
Structure of the Type III Pantothenate Kinase from Bacillus anthracis at 2.0 A Resolution: Implications for Coenzyme A-Dependent Redox Biology(,)., Nicely NI, Parsonage D, Paige C, Newton GL, Fahey RC, Leonardi R, Jackowski S, Mallett TC, Claiborne A, Biochemistry. 2007 Mar 20;46(11):3234-3245. Epub 2007 Feb 27. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17323930 17323930]
Structure of the type III pantothenate kinase from Bacillus anthracis at 2.0 A resolution: implications for coenzyme A-dependent redox biology., Nicely NI, Parsonage D, Paige C, Newton GL, Fahey RC, Leonardi R, Jackowski S, Mallett TC, Claiborne A, Biochemistry. 2007 Mar 20;46(11):3234-45. Epub 2007 Feb 27. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17323930 17323930]
[[Category: Bacillus anthracis]]
[[Category: Bacillus anthracis]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Nicely, N.I.]]
[[Category: Nicely, N I.]]
[[Category: EGL]]
[[Category: EGL]]
[[Category: anthrax]]
[[Category: anthrax]]
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[[Category: type iii pantothenate kinase]]
[[Category: type iii pantothenate kinase]]


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