1s19

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[[Image:1s19.gif|left|200px]]
[[Image:1s19.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1s19 |SIZE=350|CAPTION= <scene name='initialview01'>1s19</scene>, resolution 2.1&Aring;
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The line below this paragraph, containing "STRUCTURE_1s19", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=MC9:CALCIPOTRIOL'>MC9</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY=
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or leave the SCENE parameter empty for the default display.
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|GENE= VDR, NR1I1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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|DOMAIN=
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{{STRUCTURE_1s19| PDB=1s19 | SCENE= }}
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|RELATEDENTRY=[[1db1|1DB1]], [[1ie8|1IE8]], [[1ie9|1IE9]], [[1s0z|1S0Z]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1s19 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1s19 OCA], [http://www.ebi.ac.uk/pdbsum/1s19 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1s19 RCSB]</span>
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}}
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'''Crystal structure of VDR ligand binding domain complexed to calcipotriol.'''
'''Crystal structure of VDR ligand binding domain complexed to calcipotriol.'''
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[[Category: Tocchini-Valentini, G.]]
[[Category: Tocchini-Valentini, G.]]
[[Category: Wurtz, J M.]]
[[Category: Wurtz, J M.]]
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[[Category: alpha-helical sandwich]]
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[[Category: Alpha-helical sandwich]]
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[[Category: nuclear receptor]]
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[[Category: Nuclear receptor]]
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[[Category: transcription regulation]]
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[[Category: Transcription regulation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 08:10:06 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:35:57 2008''
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Revision as of 05:10, 3 May 2008

Template:STRUCTURE 1s19

Crystal structure of VDR ligand binding domain complexed to calcipotriol.


Overview

The plethora of actions of 1alpha,25(OH)(2)D(3) in various systems suggested wide clinical applications of vitamin D nuclear receptor (VDR) ligands in treatments of inflammation, dermatological indication, osteoporosis, cancers, and autoimmune diseases. More than 3000 vitamin D analogues have been synthesized in order to reduce the calcemic side effects while maintaining the transactivation potency of these ligands. Here, we report the crystal structures of VDR ligand binding domain bound to two vitamin D agonists of therapeutical interest, calcipotriol and seocalcitol, which are characterized by their side chain modifications. These structures show the conservation of the VDR structure and the adaptation of the side chain anchored by hydroxyl moieties. The structure of VDR-calcipotriol helps us to understand the structural basis for for the switching of calcipotriol to a receptor antagonist by further side chain modification. The VDR-seocalcitol structure, in comparison with the structure of VDR-KH1060, a superagonist ligand closely related to seocalcitol, shows adaptation of the D ring and position of C-21 in order to adapt its more rigid side chain.

About this Structure

1S19 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Crystal structures of the vitamin D nuclear receptor liganded with the vitamin D side chain analogues calcipotriol and seocalcitol, receptor agonists of clinical importance. Insights into a structural basis for the switching of calcipotriol to a receptor antagonist by further side chain modification., Tocchini-Valentini G, Rochel N, Wurtz JM, Moras D, J Med Chem. 2004 Apr 8;47(8):1956-61. PMID:15055995 Page seeded by OCA on Sat May 3 08:10:06 2008

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