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Sandbox GGC6
From Proteopedia
(Difference between revisions)
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== Disease == | == Disease == | ||
| - | <ref> | + | 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. <ref>PMID: 25427968.</ref> | ||
== Relevance == | == Relevance == | ||
Revision as of 19:06, 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
- ↑ PMID: 25427968.
