1vrw: Difference between revisions

New page: left|200px<br /><applet load="1vrw" size="450" color="white" frame="true" align="right" spinBox="true" caption="1vrw, resolution 2.40Å" /> '''Crystal structure an...
 
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[[Image:1vrw.gif|left|200px]]<br /><applet load="1vrw" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1vrw.gif|left|200px]]<br /><applet load="1vrw" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1vrw, resolution 2.40&Aring;" />
caption="1vrw, resolution 2.40&Aring;" />
'''Crystal structure analysis of plasmodium falciparum enoyl-acyl-carrier-protein reductase with nadh'''<br />
'''Crystal structure analysis of plasmodium falciparum enoyl-acyl-carrier-protein reductase with nadh'''<br />


==Overview==
==Overview==
The human malaria parasite Plasmodium falciparum synthesizes fatty acids, using a type II pathway that is absent in humans. The final step in fatty, acid elongation is catalyzed by enoyl acyl carrier protein reductase, a, validated antimicrobial drug target. Here, we report the cloning and, expression of the P. falciparum enoyl acyl carrier protein reductase gene, which encodes a 50-kDa protein (PfENR) predicted to target to the unique, parasite apicoplast. Purified PfENR was crystallized, and its structure, resolved as a binary complex with NADH, a ternary complex with triclosan, and NAD(+), and as ternary complexes bound to the triclosan analogs 1 and, 2 with NADH. Novel structural features were identified in the PfENR, binding loop region that most closely resembled bacterial homologs;, elsewhere the protein was similar to ENR from the plant Brassica napus, (root mean square for Calphas, 0.30 A). Triclosan and its analogs 1 and 2, killed multidrug-resistant strains of intra-erythrocytic P. falciparum, parasites at sub to low micromolar concentrations in vitro. These data, define the structural basis of triclosan binding to PfENR and will, facilitate structure-based optimization of PfENR inhibitors.
The human malaria parasite Plasmodium falciparum synthesizes fatty acids using a type II pathway that is absent in humans. The final step in fatty acid elongation is catalyzed by enoyl acyl carrier protein reductase, a validated antimicrobial drug target. Here, we report the cloning and expression of the P. falciparum enoyl acyl carrier protein reductase gene, which encodes a 50-kDa protein (PfENR) predicted to target to the unique parasite apicoplast. Purified PfENR was crystallized, and its structure resolved as a binary complex with NADH, a ternary complex with triclosan and NAD(+), and as ternary complexes bound to the triclosan analogs 1 and 2 with NADH. Novel structural features were identified in the PfENR binding loop region that most closely resembled bacterial homologs; elsewhere the protein was similar to ENR from the plant Brassica napus (root mean square for Calphas, 0.30 A). Triclosan and its analogs 1 and 2 killed multidrug-resistant strains of intra-erythrocytic P. falciparum parasites at sub to low micromolar concentrations in vitro. These data define the structural basis of triclosan binding to PfENR and will facilitate structure-based optimization of PfENR inhibitors.


==About this Structure==
==About this Structure==
1VRW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Plasmodium_falciparum Plasmodium falciparum] with NAD as [http://en.wikipedia.org/wiki/ligand ligand]. This structure superseeds the now removed PDB entry 1NHD. Active as [http://en.wikipedia.org/wiki/Enoyl-[acyl-carrier-protein]_reductase_(NADH) Enoyl-[acyl-carrier-protein] reductase (NADH)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.3.1.9 1.3.1.9] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1VRW OCA].  
1VRW is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Plasmodium_falciparum Plasmodium falciparum] with <scene name='pdbligand=NAD:'>NAD</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. This structure supersedes the now removed PDB entry 1NHD. Active as [http://en.wikipedia.org/wiki/Enoyl-[acyl-carrier-protein]_reductase_(NADH) Enoyl-[acyl-carrier-protein] reductase (NADH)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.3.1.9 1.3.1.9] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1VRW OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Bittman, R.]]
[[Category: Bittman, R.]]
[[Category: Fidock, D.A.]]
[[Category: Fidock, D A.]]
[[Category: Jr., W.R.Jacobs.]]
[[Category: Jr., W R.Jacobs.]]
[[Category: Kuo, M.]]
[[Category: Kuo, M.]]
[[Category: Perozzo, R.]]
[[Category: Perozzo, R.]]
[[Category: Sacchettini, J.C.]]
[[Category: Sacchettini, J C.]]
[[Category: Sidhu, A.S.]]
[[Category: Sidhu, A S.]]
[[Category: Valiyaveettil, J.T.]]
[[Category: Valiyaveettil, J T.]]
[[Category: NAD]]
[[Category: NAD]]
[[Category: nadh]]
[[Category: nadh]]
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[[Category: short chain dehydrogenase reductase]]
[[Category: short chain dehydrogenase reductase]]


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