2ee2
From Proteopedia
(Difference between revisions)
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===Solution structures of the fn3 domain of human contactin 1=== | ===Solution structures of the fn3 domain of human contactin 1=== | ||
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| + | ==Disease== | ||
| + | Known disease associated with this structure: Myopathy, congenital, Compton-North OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600016 600016]] | ||
==About this Structure== | ==About this Structure== | ||
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[[Category: Structural genomic]] | [[Category: Structural genomic]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 14:46:39 2009'' |
Revision as of 12:46, 17 February 2009
Solution structures of the fn3 domain of human contactin 1
Disease
Known disease associated with this structure: Myopathy, congenital, Compton-North OMIM:[600016]
About this Structure
2EE2 is a 1 chain structure of sequence from Homo sapiens. Full experimental information is available from OCA.
Page seeded by OCA on Tue Feb 17 14:46:39 2009
Categories: Homo sapiens | Inoue, M. | Kigawa, T. | Koshiba, S. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Sato, M. | Tochio, N. | Yokoyama, S. | Glycoprotein gp135 | National project on protein structural and functional analyse | Neural cell surface protein f3 | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Signaling protein | Structural genomic
