1dvn: Difference between revisions

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[[Image:1dvn.jpg|left|200px]]
{{Seed}}
[[Image:1dvn.png|left|200px]]


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{{STRUCTURE_1dvn|  PDB=1dvn  |  SCENE=  }}  
{{STRUCTURE_1dvn|  PDB=1dvn  |  SCENE=  }}  


'''LATENT FORM OF PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1)'''
===LATENT FORM OF PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1)===




==Overview==
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Serpins exhibit a range of physiological roles and can contribute to certain disease states dependent on their various conformations. Understanding the mechanisms of the large-scale conformational reorganizations of serpins may lead to a better understanding of their roles in various cardiovascular diseases. We have studied the serpin, plasminogen activator inhibitor 1 (PAI-1), in both the active and the latent state and found that anionic halide ions may play a role in the active-to-latent structural transition. Crystallographic analysis of a stable mutant form of active PAI-1 identified an anion-binding site between the central beta-sheet and a small surface domain. A chloride ion was modeled in this site, and its identity was confirmed by soaking crystals in a bromide-containing solution and calculating a crystallographic difference map. The anion thus located forms a 4-fold ligated linchpin that tethers the surface domain to the central beta-sheet into which the reactive center loop must insert during the active-to-latent transition. Timecourse experiments measuring active PAI-1 stability in the presence of various halide ions showed a clear trend for stabilization of the active form with F(-) &gt; Cl(-) &gt; Br(-) &gt;&gt; I(-). We propose that the "stickiness" of this pin (i.e., the electronegativity of the anion) contributes to the energetics of the active-to-latent transition in the PAI-1 serpin.
The line below this paragraph, {{ABSTRACT_PUBMED_10913251}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_10913251}}


==About this Structure==
==About this Structure==
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[[Category: Pai-1]]
[[Category: Pai-1]]
[[Category: Serpin]]
[[Category: Serpin]]
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