2ch1: Difference between revisions

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[[Image:2ch1.gif|left|200px]]<br /><applet load="2ch1" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:2ch1.gif|left|200px]]<br /><applet load="2ch1" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="2ch1, resolution 2.40&Aring;" />
caption="2ch1, resolution 2.40&Aring;" />
'''STRUCTURE OF ANOPHELES GAMBIAE 3-HYDROXYKYNURENINE TRANSAMINASE'''<br />
'''STRUCTURE OF ANOPHELES GAMBIAE 3-HYDROXYKYNURENINE TRANSAMINASE'''<br />
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==About this Structure==
==About this Structure==
2CH1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Anopheles_gambiae Anopheles gambiae] with LLP and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Gol Binding Site For Chain D'>AC1</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2CH1 OCA].  
2CH1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Anopheles_gambiae Anopheles gambiae] with <scene name='pdbligand=LLP:'>LLP</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Gol+Binding+Site+For+Chain+D'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2CH1 OCA].  


==Reference==
==Reference==
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[[Category: transferase]]
[[Category: transferase]]


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Revision as of 08:35, 3 February 2008

File:2ch1.gif


2ch1, resolution 2.40Å

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STRUCTURE OF ANOPHELES GAMBIAE 3-HYDROXYKYNURENINE TRANSAMINASE

Overview

In Anopheles gambiae, the vector for the most deadly malaria parasite, Plasmodium falciparum, xanthurenic acid (XA) plays a key role in parasite, gametogenesis and fertility. In mosquitoes, XA is produced by, transamination of 3-hydroxykynurenine (3-HK), a reaction that represents, the main route to prevent the accumulation of the potentially toxic 3-HK, excess. Interfering with XA metabolism in A. gambiae therefore appears an, attractive avenue for the development of malaria transmission-blocking, drugs and insecticides. We have determined the crystal structure of A., gambiae 3-HK transaminase in its pyridoxal 5'-phosphate form and in, complex with a newly synthesized competitive enzyme inhibitor. Structural, inspection of the enzyme active site reveals the key molecular, determinants for ligand recognition and catalysis. Major contributions, toward inhibitor binding are provided by a salt bridge between the, inhibitor carboxylate and Arg-356 and by a remarkable hydrogen bond, network involving the anthranilic moiety of the inhibitor and backbone, atoms of residues Gly-25 and Asn-44. This study may be useful for the, structure-based design of specific enzyme inhibitors of potential interest, as antimalarial agents.

About this Structure

2CH1 is a Single protein structure of sequence from Anopheles gambiae with LLP and GOL as ligands. Known structural/functional Site: AC1. Full crystallographic information is available from OCA.

Reference

Crystal structure of the Anopheles gambiae 3-hydroxykynurenine transaminase., Rossi F, Garavaglia S, Giovenzana GB, Arca B, Li J, Rizzi M, Proc Natl Acad Sci U S A. 2006 Apr 11;103(15):5711-6. Epub 2006 Apr 3. PMID:16585514

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