1dvm: Difference between revisions
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
[[Image:1dvm.gif|left|200px]] | [[Image:1dvm.gif|left|200px]] | ||
<!-- | |||
The line below this paragraph, containing "STRUCTURE_1dvm", creates the "Structure Box" on the page. | |||
You may change the PDB parameter (which sets the PDB file loaded into the applet) | |||
or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |||
or leave the SCENE parameter empty for the default display. | |||
--> | |||
{{STRUCTURE_1dvm| PDB=1dvm | SCENE= }} | |||
}} | |||
'''ACTIVE FORM OF HUMAN PAI-1''' | '''ACTIVE FORM OF HUMAN PAI-1''' | ||
Line 29: | Line 26: | ||
[[Category: Matthews, D J.]] | [[Category: Matthews, D J.]] | ||
[[Category: Stout, T J.]] | [[Category: Stout, T J.]] | ||
[[Category: | [[Category: Inhibitor]] | ||
[[Category: | [[Category: Pai-1]] | ||
[[Category: | [[Category: Serpin]] | ||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 14:20:09 2008'' | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on |
Revision as of 14:20, 2 May 2008
ACTIVE FORM OF HUMAN PAI-1
OverviewOverview
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(-) > Cl(-) > Br(-) >> 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.
About this StructureAbout this Structure
1DVM is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
Structures of active and latent PAI-1: a possible stabilizing role for chloride ions., Stout TJ, Graham H, Buckley DI, Matthews DJ, Biochemistry. 2000 Jul 25;39(29):8460-9. PMID:10913251 Page seeded by OCA on Fri May 2 14:20:09 2008