Sandbox GGC6
From Proteopedia
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== Disease ==  | == Disease ==  | ||
Congenital afibrinogenemia (CAFBN)  | Congenital afibrinogenemia (CAFBN)  | ||
| - | + |  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  | |
| - | when thrombin cleaves the site of fibrinopeptide leads to alpha- dysfibrinogenemias.   | + | when thrombin cleaves the site of fibrinopeptide leads to alpha- dysfibrinogenemias.   | 
== Relevance ==  | == Relevance ==  | ||
Revision as of 19:07, 13 November 2020
Fibrinogen alpha chain
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References
- ↑ 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
 - ↑ 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
 - ↑ 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
 
