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1cqp

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|PDB= 1cqp |SIZE=350|CAPTION= <scene name='initialview01'>1cqp</scene>, resolution 2.60&Aring;
|PDB= 1cqp |SIZE=350|CAPTION= <scene name='initialview01'>1cqp</scene>, resolution 2.60&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene> and <scene name='pdbligand=803:LOVASTATIN'>803</scene>
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|LIGAND= <scene name='pdbligand=803:LOVASTATIN'>803</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>
|ACTIVITY=
|ACTIVITY=
|GENE=
|GENE=
 +
|DOMAIN=
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|RELATEDENTRY=[[1lfa|1LFA]], [[1zon|1ZON]], [[1zoo|1ZOO]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1cqp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1cqp OCA], [http://www.ebi.ac.uk/pdbsum/1cqp PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1cqp RCSB]</span>
}}
}}
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[[Category: Weitz-Schmidt, G.]]
[[Category: Weitz-Schmidt, G.]]
[[Category: Welzenbach, K.]]
[[Category: Welzenbach, K.]]
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[[Category: 803]]
 
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[[Category: MG]]
 
[[Category: rossman fold]]
[[Category: rossman fold]]
[[Category: structural basis for lfa-1 inhibition]]
[[Category: structural basis for lfa-1 inhibition]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:27:40 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:26:45 2008''

Revision as of 16:26, 30 March 2008


PDB ID 1cqp

Drag the structure with the mouse to rotate
, resolution 2.60Å
Ligands: ,
Related: 1LFA, 1ZON, 1ZOO


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



CRYSTAL STRUCTURE ANALYSIS OF THE COMPLEX LFA-1 (CD11A) I-DOMAIN / LOVASTATIN AT 2.6 A RESOLUTION


Overview

The lymphocyte function-associated antigen (LFA-1) belongs to the family of beta2-integrins and plays an important role in T-cell activation and leukocyte migration to sites of inflammation. We report here that lovastatin, a drug clinically used for lowering cholesterol levels, inhibits the interaction of human LFA-1 with its counter-receptor intercellular adhesion molecule-1. Using nuclear magnetic resonance spectroscopy and X-ray crystallography we show that the inhibitor binds to a highly conserved domain of the LFA-1 alpha-chain called the I-domain. The first three-dimensional structure of an integrin inhibitor bound to its receptor reveals atomic details for a hitherto unknown mode of LFA-1 inhibition. It also sheds light into possible mechanisms of LFA-1 mediated signalling and will support the design of novel anti-adhesive and immunosuppressive drugs.

About this Structure

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

Reference

Structural basis for LFA-1 inhibition upon lovastatin binding to the CD11a I-domain., Kallen J, Welzenbach K, Ramage P, Geyl D, Kriwacki R, Legge G, Cottens S, Weitz-Schmidt G, Hommel U, J Mol Biol. 1999 Sep 10;292(1):1-9. PMID:10493852

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