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Molecular basis of factor IXa recognition by heparin-activated antithrombin revealed by a 1.7-Å structure of the ternary complex

Factor (f) IXa is a critical enzyme for the formation of stable blood clots, and its deficiency results in hemophilia. The enzyme functions at the confluence of the intrinsic and extrinsic pathways by binding to fVIIIa and rapidly generating fXa. In spite of its importance, little is known about how...

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Bibliografiset tiedot
Päätekijät: Johnson, Daniel J. D., Langdown, Jonathan, Huntington, James A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 2010
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2818950/
https://ncbi.nlm.nih.gov/pubmed/20080729
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0910144107
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