1rg6: Difference between revisions

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|ACTIVITY=  
|ACTIVITY=  
|GENE= p63 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= p63 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1rg6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1rg6 OCA], [http://www.ebi.ac.uk/pdbsum/1rg6 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1rg6 RCSB]</span>
}}
}}


'''Solution structure of the C-terminal domain of p63'''
'''Solution structure of the C-terminal domain of p63'''


==Disease==
Known diseases associated with this structure: ADULT syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]], Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]], Hay-Wells syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]], Limb-mammary syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]], Orofacial cleft 8 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]], Rapp-Hodgkin syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]], Split-hand/foot malformation, type 4 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603273 603273]]


==About this Structure==
==About this Structure==
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[[Category: p73 sam-like domain]]
[[Category: p73 sam-like domain]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 13:51:09 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:27:42 2008''
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