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2dl1
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(New page: 200px<br /> <applet load="2dl1" size="450" color="white" frame="true" align="right" spinBox="true" caption="2dl1" /> '''Solution structure of the MIT domain from h...)
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Revision as of 19:28, 12 November 2007
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Solution structure of the MIT domain from human Spartin
Disease
Known disease associated with this structure: Troyer syndrome OMIM:[607111]
About this Structure
2DL1 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Page seeded by OCA on Mon Nov 12 21:35:23 2007
Categories: Homo sapiens | Single protein | Hayashi, F. | RSGI, RIKEN.Structural.Genomics/Proteomics.Initiative. | Suetake, T. | Yokoyama, S. | Mit | National project on protein structural and functional analyses | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Spartin | Spg20 | Structural genomics
