1emn
From Proteopedia
(Difference between revisions)
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==About this Structure== | ==About this Structure== | ||
- | 1EMN is a | + | 1EMN is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EMN OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:8653794</ref><references group="xtra"/> | |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Single protein]] | ||
[[Category: Campbell, I D.]] | [[Category: Campbell, I D.]] | ||
[[Category: Downing, A K.]] | [[Category: Downing, A K.]] | ||
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[[Category: Signal]] | [[Category: Signal]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 13:06:44 2009'' |
Revision as of 11:06, 16 February 2009
Contents |
NMR STUDY OF A PAIR OF FIBRILLIN CA2+ BINDING EPIDERMAL GROWTH FACTOR-LIKE DOMAINS, MINIMIZED AVERAGE STRUCTURE
Template:ABSTRACT PUBMED 8653794
Disease
Known disease associated with this structure: Aortic aneurysm, ascending, and dissection OMIM:[134797], Ectopia lentis, familial OMIM:[134797], MASS syndrome OMIM:[134797], Marfan syndrome OMIM:[134797], Shprintzen-Goldberg syndrome OMIM:[134797], Weill-Marchesani syndrome, dominant OMIM:[134797]
About this Structure
1EMN is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
- Downing AK, Knott V, Werner JM, Cardy CM, Campbell ID, Handford PA. Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders. Cell. 1996 May 17;85(4):597-605. PMID:8653794
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