1pn5: Difference between revisions

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|ACTIVITY=  
|ACTIVITY=  
|GENE= NALP1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= NALP1 ([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=1pn5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1pn5 OCA], [http://www.ebi.ac.uk/pdbsum/1pn5 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1pn5 RCSB]</span>
}}
}}


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==Disease==
==Disease==
Known diseases associated with this structure: Cramps, familial, potassium-aggravated OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603967 603967]], Hyperkalemic periodic paralysis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603967 603967]], Hypokalemic periodic paralysis OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603967 603967]], Myasthenic syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603967 603967]], Myotonia congenita, atypical, acetazolamide-responsive OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603967 603967]], Paramyotonia congenita OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603967 603967]], Vitiligo-associated multiple autoimmune disease susceptibility 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606636 606636]]
Known disease associated with this structure: Vitiligo-associated multiple autoimmune disease susceptibility 1 OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606636 606636]]


==About this Structure==
==About this Structure==
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[[Category: 5 alpha-helix bundle]]
[[Category: 5 alpha-helix bundle]]


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