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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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Bibliografische gegevens
Hoofdauteurs: Johnson, Daniel J. D., Langdown, Jonathan, Huntington, James A.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: National Academy of Sciences 2010
Onderwerpen:
Online toegang: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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