1sn6: Difference between revisions

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{{Seed}}
[[Image:1sn6.png|left|200px]]
[[Image:1sn6.png|left|200px]]


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{{ABSTRACT_PUBMED_15713488}}
{{ABSTRACT_PUBMED_15713488}}
==Disease==
Known disease associated with this structure: Combined SAP deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]], Gaucher disease, atypical OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]], Krabbe disease, atypical OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]], Metachromatic leukodystrophy due to SAP-b deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801 176801]]


==About this Structure==
==About this Structure==
1SN6 is a 1 chain 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=1SN6 OCA].  
[[1sn6]] is a 1 chain structure with 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=1SN6 OCA].  


==Reference==
==Reference==
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[[Category: All alpha-helice]]
[[Category: All alpha-helice]]
[[Category: Alpha-helices connected by turn]]
[[Category: Alpha-helices connected by turn]]
 
[[Category: Membrane protein]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 08:48:39 2009''
Retrieved from "https://proteopedia.org/1sn6"