2dl1
From Proteopedia
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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 Thu Feb 21 16:59:55 2008
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
