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Engineering Functional Antithrombin Exosites in α(1)-Proteinase Inhibitor That Specifically Promote the Inhibition of Factor Xa and Factor IXa

We have previously shown that residues Tyr-253 and Glu-255 in the serpin antithrombin function as exosites to promote the inhibition of factor Xa and factor IXa when the serpin is conformationally activated by heparin. Here we show that functional exosites can be engineered at homologous positions i...

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Hlavní autoři: Izaguirre, Gonzalo, Rezaie, Alireza R., Olson, Steven T.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Biochemistry and Molecular Biology 2009
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2615528/
https://ncbi.nlm.nih.gov/pubmed/19010776
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M807340200
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