2gq3: Difference between revisions

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[[Image:2gq3.gif|left|200px]]<br /><applet load="2gq3" size="350" color="white" frame="true" align="right" spinBox="true"
[[Image:2gq3.gif|left|200px]]
caption="2gq3, resolution 2.30&Aring;" />
 
'''mycobacterium tuberculosis malate synthase in complex with magnesium, malate, and coenzyme A'''<br />
{{Structure
|PDB= 2gq3 |SIZE=350|CAPTION= <scene name='initialview01'>2gq3</scene>, resolution 2.30&Aring;
|SITE=
|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=MLT:MALATE+ION'>MLT</scene>, <scene name='pdbligand=COA:COENZYME+A'>COA</scene> and <scene name='pdbligand=EPE:4-(2-HYDROXYETHYL)-1-PIPERAZINE ETHANESULFONIC ACID'>EPE</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/Malate_synthase Malate synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.9 2.3.3.9]
|GENE= glcB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1773 Mycobacterium tuberculosis])
}}
 
'''mycobacterium tuberculosis malate synthase in complex with magnesium, malate, and coenzyme A'''
 


==Overview==
==Overview==
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==About this Structure==
==About this Structure==
2GQ3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis] with <scene name='pdbligand=MG:'>MG</scene>, <scene name='pdbligand=MLT:'>MLT</scene>, <scene name='pdbligand=COA:'>COA</scene> and <scene name='pdbligand=EPE:'>EPE</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Malate_synthase Malate synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.3.9 2.3.3.9] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GQ3 OCA].  
2GQ3 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2GQ3 OCA].  


==Reference==
==Reference==
The product complex of M. tuberculosis malate synthase revisited., Anstrom DM, Remington SJ, Protein Sci. 2006 Aug;15(8):2002-7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=16877713 16877713]
The product complex of M. tuberculosis malate synthase revisited., Anstrom DM, Remington SJ, Protein Sci. 2006 Aug;15(8):2002-7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16877713 16877713]
[[Category: Malate synthase]]
[[Category: Malate synthase]]
[[Category: Mycobacterium tuberculosis]]
[[Category: Mycobacterium tuberculosis]]
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[[Category: MG]]
[[Category: MG]]
[[Category: MLT]]
[[Category: MLT]]
[[Category: coenzyme a]]
[[Category: coenzyme some]]
[[Category: tim barrel]]
[[Category: tim barrel]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:34:09 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 17:07:38 2008''

Revision as of 18:07, 20 March 2008

File:2gq3.gif


PDB ID 2gq3

Drag the structure with the mouse to rotate
, resolution 2.30Å
Ligands: , , and
Gene: glcB (Mycobacterium tuberculosis)
Activity: Malate synthase, with EC number 2.3.3.9
Coordinates: save as pdb, mmCIF, xml



mycobacterium tuberculosis malate synthase in complex with magnesium, malate, and coenzyme A


OverviewOverview

Enzymes of the glyoxylate shunt have been implicated as virulence factors in several pathogenic organisms, notably Mycobacterium tuberculosis and Candida albicans. Malate synthase has thus emerged as a promising target for design of anti-microbial agents. For this effort, it is essential to have reliable models for enzyme:substrate complexes. A 2.7 Angstroms resolution crystal structure for M. tuberculosis malate synthase in the ternary complex with magnesium, malate, and coenzyme A has been previously described. However, some unusual aspects of malate and Mg(++) binding prompted an independent determination of the structure at 2.3 Angstroms resolution, in the presence of saturating concentrations of malate. The electron density map of the complex reveals the position and conformation of coenzyme A to be unchanged from that found in the previous study. However, the coordination of Mg(++) and orientation of bound malate within the active site are different. The revised position of bound malate is consistent with a reaction mechanism that does not require reorientation of the electrophilic substrate during the catalytic cycle, while the revised Mg(++) coordination is octahedral, as expected. The results should be useful in the design of malate synthase inhibitors.

About this StructureAbout this Structure

2GQ3 is a Single protein structure of sequence from Mycobacterium tuberculosis. Full crystallographic information is available from OCA.

ReferenceReference

The product complex of M. tuberculosis malate synthase revisited., Anstrom DM, Remington SJ, Protein Sci. 2006 Aug;15(8):2002-7. PMID:16877713

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