2ij5: Difference between revisions

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[[Image:2ij5.gif|left|200px]]
[[Image:2ij5.gif|left|200px]]


{{Structure
<!--
|PDB= 2ij5 |SIZE=350|CAPTION= <scene name='initialview01'>2ij5</scene>, resolution 1.60&Aring;
The line below this paragraph, containing "STRUCTURE_2ij5", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=HEM:PROTOPORPHYRIN+IX+CONTAINING+FE'>HEM</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=
or leave the SCENE parameter empty for the default display.
|GENE= cyp121 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1773 Mycobacterium tuberculosis])
-->
|DOMAIN=
{{STRUCTURE_2ij5| PDB=2ij5  | SCENE= }}  
|RELATEDENTRY=[[1n40|1N40]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ij5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ij5 OCA], [http://www.ebi.ac.uk/pdbsum/2ij5 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ij5 RCSB]</span>
}}


'''Crystal structure of cytochrome P450 CYP121, P212121 space group'''
'''Crystal structure of cytochrome P450 CYP121, P212121 space group'''
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[[Category: Leys, D.]]
[[Category: Leys, D.]]
[[Category: Roujeinikova, A.]]
[[Category: Roujeinikova, A.]]
[[Category: azole ligation]]
[[Category: Azole ligation]]
[[Category: cyp121]]
[[Category: Cyp121]]
[[Category: cytochrome p450]]
[[Category: Cytochrome p450]]
[[Category: fluconazole]]
[[Category: Fluconazole]]
[[Category: tuberculosis]]
[[Category: Tuberculosis]]
 
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Revision as of 07:33, 4 May 2008

File:2ij5.gif

Template:STRUCTURE 2ij5

Crystal structure of cytochrome P450 CYP121, P212121 space group


OverviewOverview

Azole and triazole drugs are cytochrome P450 inhibitors widely used as fungal antibiotics and possessing potent antimycobacterial activity. We present here the crystal structure of Mycobacterium tuberculosis cytochrome P450 CYP121 in complex with the triazole drug fluconazole, revealing a new azole heme ligation mode. In contrast to other structurally characterized cytochrome P450 azole complexes, where the azole nitrogen directly coordinates the heme iron, in CYP121 fluconazole does not displace the aqua sixth heme ligand but occupies a position that allows formation of a direct hydrogen bond to the aqua sixth heme ligand. Direct ligation of fluconazole to the heme iron is observed in a minority of CYP121 molecules, albeit with severe deviations from ideal geometry due to close contacts with active site residues. Analysis of both ligand-on and -off structures reveals the relative position of active site residues derived from the I-helix is a key determinant in the relative ratio of on and off states. Regardless, both ligand-bound states lead to P450 inactivation by active site occlusion. This previously unrecognized means of P450 inactivation is consistent with spectroscopic analyses in both solution and in the crystalline form and raises important questions relating to interaction of azoles with both pathogen and human P450s.

About this StructureAbout this Structure

2IJ5 is a Single protein structure of sequence from Mycobacterium tuberculosis. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure of the Mycobacterium tuberculosis P450 CYP121-fluconazole complex reveals new azole drug-P450 binding mode., Seward HE, Roujeinikova A, McLean KJ, Munro AW, Leys D, J Biol Chem. 2006 Dec 22;281(51):39437-43. Epub 2006 Oct 6. PMID:17028183 Page seeded by OCA on Sun May 4 07:33:53 2008

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