2da7
From Proteopedia
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[[Category: Koshiba, S.]] | [[Category: Koshiba, S.]] | ||
[[Category: Ohnishi, S.]] | [[Category: Ohnishi, S.]] | ||
| - | [[Category: RSGI, RIKEN | + | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] |
[[Category: Sato, M.]] | [[Category: Sato, M.]] | ||
[[Category: Yokoyama, S.]] | [[Category: Yokoyama, S.]] | ||
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[[Category: three helices with the dna binding helix-turn-helix motif]] | [[Category: three helices with the dna binding helix-turn-helix motif]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:56:41 2008'' |
Revision as of 14:56, 21 February 2008
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Solution structure of the homeobox domain of Zinc finger homeobox protein 1b (Smad interacting protein 1)
Disease
Known disease associated with this structure: Mowat-Wilson syndrome OMIM:[605802]
About this Structure
2DA7 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 16:56:41 2008
Categories: Homo sapiens | Single protein | Inoue, M. | Kigawa, T. | Koshiba, S. | Ohnishi, S. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Sato, M. | Yokoyama, S. | Homeobox domain | National project on protein structural and functional analyses | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics | Three helices with the dna binding helix-turn-helix motif
