1yuc
From Proteopedia
(New page: 200px<br /> <applet load="1yuc" size="450" color="white" frame="true" align="right" spinBox="true" caption="1yuc, resolution 1.90Å" /> '''Human Nuclear Recep...) |
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- | [[Image:1yuc.gif|left|200px]]<br /> | + | [[Image:1yuc.gif|left|200px]]<br /><applet load="1yuc" size="350" color="white" frame="true" align="right" spinBox="true" |
- | <applet load="1yuc" size=" | + | |
caption="1yuc, resolution 1.90Å" /> | caption="1yuc, resolution 1.90Å" /> | ||
'''Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to Phospholipid and a Fragment of Human SHP'''<br /> | '''Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to Phospholipid and a Fragment of Human SHP'''<br /> | ||
==Overview== | ==Overview== | ||
- | The human nuclear receptor liver receptor homolog 1 (hLRH-1) plays an | + | The human nuclear receptor liver receptor homolog 1 (hLRH-1) plays an important role in the development of breast carcinomas. This orphan receptor is efficiently downregulated by the unusual co-repressor SHP and has been thought to be ligand-independent. We present the crystal structure at a resolution of 1.9 A of the ligand-binding domain of hLRH-1 in complex with the NR box 1 motif of human SHP, which we find contacts the AF-2 region of hLRH-1 using selective structural motifs. Electron density indicates phospholipid bound within the ligand-binding pocket, which we confirm using mass spectrometry of solvent-extracted samples. We further show that pocket mutations reduce phospholipid binding and receptor activity in vivo. Our results indicate that hLRH-1's control of gene expression is mediated by phospholipid binding, and establish hLRH-1 as a novel target for compounds designed to slow breast cancer development. |
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
- | 1YUC is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with EPH and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http:// | + | 1YUC is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=EPH:'>EPH</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1YUC OCA]. |
==Reference== | ==Reference== | ||
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[[Category: Choi, Y.]] | [[Category: Choi, Y.]] | ||
[[Category: Guan, Z.]] | [[Category: Guan, Z.]] | ||
- | [[Category: Hager, J | + | [[Category: Hager, J M.]] |
- | [[Category: McDonnell, D | + | [[Category: McDonnell, D P.]] |
- | [[Category: Moore, D | + | [[Category: Moore, D D.]] |
- | [[Category: Ortlund, E | + | [[Category: Ortlund, E A.]] |
- | [[Category: Raetz, C | + | [[Category: Raetz, C R.H.]] |
- | [[Category: Redinbo, M | + | [[Category: Redinbo, M R.]] |
[[Category: Safi, R.]] | [[Category: Safi, R.]] | ||
- | [[Category: Solomon, I | + | [[Category: Solomon, I H.]] |
[[Category: Tripathy, A.]] | [[Category: Tripathy, A.]] | ||
[[Category: Yoonkwang, L.]] | [[Category: Yoonkwang, L.]] | ||
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[[Category: liver receptor homologue 1; nuclear receptor ligand binding domain; lrh-1; phospholipid; shp; small heterodimer partner]] | [[Category: liver receptor homologue 1; nuclear receptor ligand binding domain; lrh-1; phospholipid; shp; small heterodimer partner]] | ||
- | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:09:09 2008'' |
Revision as of 14:09, 21 February 2008
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Human Nuclear Receptor Liver Receptor Homologue-1, LRH-1, Bound to Phospholipid and a Fragment of Human SHP
Contents |
Overview
The human nuclear receptor liver receptor homolog 1 (hLRH-1) plays an important role in the development of breast carcinomas. This orphan receptor is efficiently downregulated by the unusual co-repressor SHP and has been thought to be ligand-independent. We present the crystal structure at a resolution of 1.9 A of the ligand-binding domain of hLRH-1 in complex with the NR box 1 motif of human SHP, which we find contacts the AF-2 region of hLRH-1 using selective structural motifs. Electron density indicates phospholipid bound within the ligand-binding pocket, which we confirm using mass spectrometry of solvent-extracted samples. We further show that pocket mutations reduce phospholipid binding and receptor activity in vivo. Our results indicate that hLRH-1's control of gene expression is mediated by phospholipid binding, and establish hLRH-1 as a novel target for compounds designed to slow breast cancer development.
Disease
Known diseases associated with this structure: Obesity, mild, early-onset OMIM:[604630]
About this Structure
1YUC is a Protein complex structure of sequences from Homo sapiens with and as ligands. Full crystallographic information is available from OCA.
Reference
Modulation of human nuclear receptor LRH-1 activity by phospholipids and SHP., Ortlund EA, Lee Y, Solomon IH, Hager JM, Safi R, Choi Y, Guan Z, Tripathy A, Raetz CR, McDonnell DP, Moore DD, Redinbo MR, Nat Struct Mol Biol. 2005 Apr;12(4):357-63. Epub 2005 Feb 22. PMID:15723037
Page seeded by OCA on Thu Feb 21 16:09:09 2008
Categories: Homo sapiens | Protein complex | Choi, Y. | Guan, Z. | Hager, J M. | McDonnell, D P. | Moore, D D. | Ortlund, E A. | Raetz, C R.H. | Redinbo, M R. | Safi, R. | Solomon, I H. | Tripathy, A. | Yoonkwang, L. | EPH | GOL | Liver receptor homologue 1; nuclear receptor ligand binding domain; lrh-1; phospholipid; shp; small heterodimer partner