1tmx: Difference between revisions
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[[Image:1tmx.gif|left|200px]] | [[Image:1tmx.gif|left|200px]] | ||
'''Crystal structure of hydroxyquinol 1,2-dioxygenase from Nocardioides Simplex 3E''' | {{Structure | ||
|PDB= 1tmx |SIZE=350|CAPTION= <scene name='initialview01'>1tmx</scene>, resolution 1.75Å | |||
|SITE= | |||
|LIGAND= <scene name='pdbligand=FE:FE+(III)+ION'>FE</scene>, <scene name='pdbligand=CU:COPPER+(II)+ION'>CU</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=HGX:1-HEPTADECANOYL-2-TRIDECANOYL-3-GLYCEROL-PHOSPHONYL+CHOLINE'>HGX</scene> and <scene name='pdbligand=BEZ:BENZOIC ACID'>BEZ</scene> | |||
|ACTIVITY= [http://en.wikipedia.org/wiki/Hydroxyquinol_1,2-dioxygenase Hydroxyquinol 1,2-dioxygenase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.13.11.37 1.13.11.37] | |||
|GENE= | |||
}} | |||
'''Crystal structure of hydroxyquinol 1,2-dioxygenase from Nocardioides Simplex 3E''' | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
1TMX is a [ | 1TMX is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Pimelobacter_simplex Pimelobacter simplex]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1TMX OCA]. | ||
==Reference== | ==Reference== | ||
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation., Ferraroni M, Seifert J, Travkin VM, Thiel M, Kaschabek S, Scozzafava A, Golovleva L, Schlomann M, Briganti F, J Biol Chem. 2005 Jun 3;280(22):21144-54. Epub 2005 Mar 16. PMID:[http:// | Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation., Ferraroni M, Seifert J, Travkin VM, Thiel M, Kaschabek S, Scozzafava A, Golovleva L, Schlomann M, Briganti F, J Biol Chem. 2005 Jun 3;280(22):21144-54. Epub 2005 Mar 16. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15772073 15772073] | ||
[[Category: Hydroxyquinol 1,2-dioxygenase]] | [[Category: Hydroxyquinol 1,2-dioxygenase]] | ||
[[Category: Pimelobacter simplex]] | [[Category: Pimelobacter simplex]] | ||
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[[Category: beta barrel]] | [[Category: beta barrel]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:20:30 2008'' |
Revision as of 15:20, 20 March 2008
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, resolution 1.75Å | |||||||
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Ligands: | , , , , and | ||||||
Activity: | Hydroxyquinol 1,2-dioxygenase, with EC number 1.13.11.37 | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Crystal structure of hydroxyquinol 1,2-dioxygenase from Nocardioides Simplex 3E
OverviewOverview
Hydroxyquinol 1,2-dioxygenase (1,2-HQD) catalyzes the ring cleavage of hydroxyquinol (1,2,4-trihydroxybenzene), a central intermediate in the degradation of aromatic compounds including a variety of particularly recalcitrant polychloro- and nitroaromatic pollutants. We report here the primary sequence determination and the analysis of the crystal structure of the 1,2-HQD from Nocardioides simplex 3E solved at 1.75 A resolution using the multiple wavelength anomalous dispersion of the two catalytic irons (1 Fe/293 amino acids). The catalytic Fe(III) coordination polyhedron composed by the side chains of Tyr164, Tyr197, His221, and His223 resembles that of the other known intradiol-cleaving dioxygenases, but several of the tertiary structure features are notably different. One of the most distinctive characteristics of the present structure is the extensive openings and consequent exposure to solvent of the upper part of the catalytic cavity arranged to favor the binding of hydroxyquinols but not catechols. A co-crystallized benzoate-like molecule is also found bound to the metal center forming a distinctive hydrogen bond network as observed previously also in 4-chlorocatechol 1,2-dioxygenase from Rhodococcus opacus 1CP. This is the first structure of an intradiol dioxygenase specialized in hydroxyquinol ring cleavage to be investigated in detail.
About this StructureAbout this Structure
1TMX is a Single protein structure of sequence from Pimelobacter simplex. Full crystallographic information is available from OCA.
ReferenceReference
Crystal structure of the hydroxyquinol 1,2-dioxygenase from Nocardioides simplex 3E, a key enzyme involved in polychlorinated aromatics biodegradation., Ferraroni M, Seifert J, Travkin VM, Thiel M, Kaschabek S, Scozzafava A, Golovleva L, Schlomann M, Briganti F, J Biol Chem. 2005 Jun 3;280(22):21144-54. Epub 2005 Mar 16. PMID:15772073
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