Sandbox GGC6

From Proteopedia

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== Disease ==
== Disease ==
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<ref>doi:10.1159/000452864</ref>
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Congenital afibrinogenemia (CAFBN)
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This is an inherited blood disorder where the blood does not clot normally. This disease is cause by truncating mutations. Changing in position arg-35
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when thrombin cleaves the site of fibrinopeptide leads to alpha- dysfibrinogenemias. <ref>PMID: 25427968.</ref>
== Relevance ==
== Relevance ==

Revision as of 19:06, 13 November 2020

Fibrinogen alpha chain

Caption for this structure

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References

  1. Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644
  3. Iwaki T, Castellino FJ. Maternal fibrinogen is necessary for embryonic development. Curr Drug Targets. 2005 Aug;6(5):535-9. doi: 10.2174/1389450054546006. PMID:16026273 doi:http://dx.doi.org/10.2174/1389450054546006
  4. PMID: 25427968.
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