1j2l
From Proteopedia
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| - | [[Image:1j2l.gif|left|200px]] | + | [[Image:1j2l.gif|left|200px]] |
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| - | '''Crystal structure of the disintegrin, trimestatin''' | + | {{Structure |
| + | |PDB= 1j2l |SIZE=350|CAPTION= <scene name='initialview01'>1j2l</scene>, resolution 1.70Å | ||
| + | |SITE= | ||
| + | |LIGAND= <scene name='pdbligand=SO4:SULFATE ION'>SO4</scene> | ||
| + | |ACTIVITY= | ||
| + | |GENE= | ||
| + | }} | ||
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| + | '''Crystal structure of the disintegrin, trimestatin''' | ||
| + | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1J2L is a [ | + | 1J2L is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Trimeresurus_flavoviridis Trimeresurus flavoviridis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1J2L OCA]. |
==Reference== | ==Reference== | ||
| - | Crystal structure of trimestatin, a disintegrin containing a cell adhesion recognition motif RGD., Fujii Y, Okuda D, Fujimoto Z, Horii K, Morita T, Mizuno H, J Mol Biol. 2003 Oct 3;332(5):1115-22. PMID:[http:// | + | Crystal structure of trimestatin, a disintegrin containing a cell adhesion recognition motif RGD., Fujii Y, Okuda D, Fujimoto Z, Horii K, Morita T, Mizuno H, J Mol Biol. 2003 Oct 3;332(5):1115-22. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/14499613 14499613] |
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Trimeresurus flavoviridis]] | [[Category: Trimeresurus flavoviridis]] | ||
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[[Category: trimestatin]] | [[Category: trimestatin]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 11:58:02 2008'' |
Revision as of 09:58, 20 March 2008
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| , resolution 1.70Å | |||||||
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| Coordinates: | save as pdb, mmCIF, xml | ||||||
Crystal structure of the disintegrin, trimestatin
Overview
Disintegrins are a family of small proteins containing an Arg-Gly-Asp (RGD) sequence motif that binds specifically to integrin receptors. Since the integrin is known to serve as the final common pathway leading to aggregation via formation of platelet-platelet bridges, disintegrins act as fibrinogen receptor antagonists. Here, we report the first crystal structure of a disintegrin, trimestatin, found in snake venom. The structure of trimestatin at 1.7A resolution reveals that a number of turns and loops form a rigid core stabilized by six disulfide bonds. Electron densities of the RGD sequence are visible clearly at the tip of a hairpin loop, in such a manner that the Arg and Asp side-chains point in opposite directions. A docking model using the crystal structure of integrin alphaVbeta3 suggests that the Arg binds to the propeller domain, and Asp to the betaA domain. This model indicates that the C-terminal region is another potential binding site with integrin receptors. In addition to the RGD sequence, the structural evidence of a C-terminal region (Arg66, Trp67 and Asn68) important for disintegrin activity allows understanding of the high affinity and selectiveness of snake venom disintegrin for integrin receptors. The crystal structure of trimestatin should provide a useful framework for designing and developing more effective drugs for controlling platelet aggregation and anti-angiogenesis cancer.
About this Structure
1J2L is a Single protein structure of sequence from Trimeresurus flavoviridis. Full crystallographic information is available from OCA.
Reference
Crystal structure of trimestatin, a disintegrin containing a cell adhesion recognition motif RGD., Fujii Y, Okuda D, Fujimoto Z, Horii K, Morita T, Mizuno H, J Mol Biol. 2003 Oct 3;332(5):1115-22. PMID:14499613
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