2ee2: 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=== | ||
==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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
