2hk7
From Proteopedia
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|PDB= 2hk7 |SIZE=350|CAPTION= <scene name='initialview01'>2hk7</scene>, resolution 2.50Å | |PDB= 2hk7 |SIZE=350|CAPTION= <scene name='initialview01'>2hk7</scene>, resolution 2.50Å | ||
|SITE= | |SITE= | ||
- | |LIGAND= <scene name='pdbligand=HG:MERCURY (II) ION'>HG</scene> | + | |LIGAND= <scene name='pdbligand=HG:MERCURY+(II)+ION'>HG</scene> |
- | |ACTIVITY= [http://en.wikipedia.org/wiki/Shikimate_dehydrogenase Shikimate dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.25 1.1.1.25] | + | |ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Shikimate_dehydrogenase Shikimate dehydrogenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.1.1.25 1.1.1.25] </span> |
|GENE= aroE ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=63363 Aquifex aeolicus]) | |GENE= aroE ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=63363 Aquifex aeolicus]) | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY=[[2ev9|2EV9]], [[1wxd|1WXD]] | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2hk7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2hk7 OCA], [http://www.ebi.ac.uk/pdbsum/2hk7 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2hk7 RCSB]</span> | ||
}} | }} | ||
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[[Category: Prabakaran, P.]] | [[Category: Prabakaran, P.]] | ||
[[Category: Yan, H.]] | [[Category: Yan, H.]] | ||
- | [[Category: HG]] | ||
[[Category: drug design]] | [[Category: drug design]] | ||
[[Category: oxidoreductase]] | [[Category: oxidoreductase]] | ||
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[[Category: shikimate pathway]] | [[Category: shikimate pathway]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:31:28 2008'' |
Revision as of 00:31, 31 March 2008
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, resolution 2.50Å | |||||||
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Ligands: | |||||||
Gene: | aroE (Aquifex aeolicus) | ||||||
Activity: | Shikimate dehydrogenase, with EC number 1.1.1.25 | ||||||
Related: | 2EV9, 1WXD
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Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Crystal structure of shikimate dehydrogenase from aquifex aeolicus in complex with mercury at 2.5 angstrom resolution
Overview
The shikimate biosynthetic pathway is essential to microorganisms, plants, and parasites but absent from mammals. Therefore, shikimate dehydrogenase (SD) and other enzymes in the pathway are attractive targets for developing nontoxic antimicrobial agents, herbicides, and antiparasite drugs. SD catalyzes the fourth reaction in the pathway, the nicotinamide adenine dinucleotide phosphate- (NADP-) dependent reduction of 3-dehydroshikimic acid to shikimic acid (SA), as well as its reverse, by the transfer of a hydride. Previous structural studies reveal that the enzyme exists in two major conformations, an open and a closed form. For the reaction to occur, it is believed that the catalytic complex assumes the closed conformation. Nonetheless, the only structure containing both SA and NADP+ exhibits an open conformation (PDB entry 2EV9). Here, we present two crystal structures of Aquifex aeolicus SD, including a ternary complex with both SA and NADP+, which assumes the closed conformation and therefore contains a catalytically competent active site. On the basis of preexisting and novel structural and biochemical data, a catalytic mechanism is proposed.
About this Structure
2HK7 is a Single protein structure of sequence from Aquifex aeolicus. Full crystallographic information is available from OCA.
Reference
Structural and biochemical analyses of shikimate dehydrogenase AroE from Aquifex aeolicus: implications for the catalytic mechanism., Gan J, Wu Y, Prabakaran P, Gu Y, Li Y, Andrykovitch M, Liu H, Gong Y, Yan H, Ji X, Biochemistry. 2007 Aug 21;46(33):9513-22. Epub 2007 Jul 25. PMID:17649975
Page seeded by OCA on Mon Mar 31 03:31:28 2008