1o1v: Difference between revisions

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[[Image:1o1v.jpg|left|200px]]
[[Image:1o1v.jpg|left|200px]]


{{Structure
<!--
|PDB= 1o1v |SIZE=350|CAPTION= <scene name='initialview01'>1o1v</scene>
The line below this paragraph, containing "STRUCTURE_1o1v", 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=TCH:TAUROCHOLIC+ACID'>TCH</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= FABP6 OR ILLBP OR ILBP ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
-->
|DOMAIN=
{{STRUCTURE_1o1v| PDB=1o1v  | SCENE= }}  
|RELATEDENTRY=[[1o1u|1O1U]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1o1v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1o1v OCA], [http://www.ebi.ac.uk/pdbsum/1o1v PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1o1v RCSB]</span>
}}


'''Human Ileal Lipid-Binding Protein (ILBP) in Complex with Cholyltaurine'''
'''Human Ileal Lipid-Binding Protein (ILBP) in Complex with Cholyltaurine'''
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[[Category: Stengelin, S.]]
[[Category: Stengelin, S.]]
[[Category: Thuering, H.]]
[[Category: Thuering, H.]]
[[Category: beta clam structure]]
[[Category: Beta clam structure]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 03:15:00 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:38:35 2008''

Revision as of 03:15, 3 May 2008

File:1o1v.jpg

Template:STRUCTURE 1o1v

Human Ileal Lipid-Binding Protein (ILBP) in Complex with Cholyltaurine


OverviewOverview

Bile acids are generated in vivo from cholesterol in the liver, and they undergo an enterohepatic circulation involving the small intestine, liver, and kidney. To understand the molecular mechanism of this transportation, it is essential to gain insight into the three-dimensional (3D) structures of proteins involved in the bile acid recycling in free and complexed form and to compare them with homologous members of this protein family. Here we report the solution structure of the human ileal lipid-binding protein (ILBP) in free form and in complex with cholyltaurine. Both structures are compared with a previously published structure of the porcine ILBP-cholylglycine complex and with related lipid-binding proteins. Protein structures were determined in solution by using two-dimensional (2D)- and 3D-homo and heteronuclear NMR techniques, leading to an almost complete resonance assignment and a significant number of distance constraints for distance geometry and restrained molecular dynamics simulations. The identification of several intermolecular distance constraints unambiguously determines the cholyltaurine-binding site. The bile acid is deeply buried within ILBP with its flexible side-chain situated close to the fatty acid portal as entry region into the inner ILBP core. This binding mode differs significantly from the orientation of cholylglycine in porcine ILBP. A detailed analysis using the GRID/CPCA strategy reveals differences in favorable interactions between protein-binding sites and potential ligands. This characterization will allow for the rational design of potential inhibitors for this relevant system.

About this StructureAbout this Structure

1O1V is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Insights into the bile acid transportation system: the human ileal lipid-binding protein-cholyltaurine complex and its comparison with homologous structures., Kurz M, Brachvogel V, Matter H, Stengelin S, Thuring H, Kramer W, Proteins. 2003 Feb 1;50(2):312-28. PMID:12486725 Page seeded by OCA on Sat May 3 03:15:00 2008

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