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1emo
From Proteopedia
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| - | [[Image:1emo. | + | {{Seed}} |
| + | [[Image:1emo.png|left|200px]] | ||
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{{STRUCTURE_1emo| PDB=1emo | SCENE= }} | {{STRUCTURE_1emo| PDB=1emo | SCENE= }} | ||
| - | + | ===NMR STUDY OF A PAIR OF FIBRILLIN CA2+ BINDING EPIDERMAL GROWTH FACTOR-LIKE DOMAINS, 22 STRUCTURES=== | |
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| - | + | The line below this paragraph, {{ABSTRACT_PUBMED_8653794}}, adds the Publication Abstract to the page | |
| + | (as it appears on PubMed at http://www.pubmed.gov), where 8653794 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_8653794}} | ||
==Disease== | ==Disease== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1EMO is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full | + | 1EMO is a [[Single protein]] 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=1EMO OCA]. |
==Reference== | ==Reference== | ||
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[[Category: Repeat]] | [[Category: Repeat]] | ||
[[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 Tue Jul 1 00:59:38 2008'' | ||
Revision as of 21:59, 30 June 2008
Contents |
NMR STUDY OF A PAIR OF FIBRILLIN CA2+ BINDING EPIDERMAL GROWTH FACTOR-LIKE DOMAINS, 22 STRUCTURES
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
1EMO is a Single protein structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Reference
Solution structure of a pair of calcium-binding epidermal growth factor-like domains: implications for the Marfan syndrome and other genetic disorders., Downing AK, Knott V, Werner JM, Cardy CM, Campbell ID, Handford PA, Cell. 1996 May 17;85(4):597-605. PMID:8653794
Page seeded by OCA on Tue Jul 1 00:59:38 2008
