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3c6m

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Revision as of 18:24, 4 May 2008 by OCA (Talk | contribs)
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Template:STRUCTURE 3c6m

Crystal structure of human spermine synthase in complex with spermine and 5-methylthioadenosine


Disease

Known disease associated with this structure: Mental retardation, X-linked, Snyder-Robinson type OMIM:[300105], Smith-Magenis syndrome OMIM:[607642]

About this Structure

3C6M is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA. Page seeded by OCA on Sun May 4 21:24:29 2008

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