2dgz
From Proteopedia
(Difference between revisions)
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[[Category: Kigawa, T.]] | [[Category: Kigawa, T.]] | ||
[[Category: Muto, Y.]] | [[Category: Muto, Y.]] | ||
| - | [[Category: RSGI, RIKEN | + | [[Category: RSGI, RIKEN Structural Genomics/Proteomics Initiative.]] |
[[Category: Shirouzu, M.]] | [[Category: Shirouzu, M.]] | ||
[[Category: Terada, T.]] | [[Category: Terada, T.]] | ||
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[[Category: structural genomics]] | [[Category: structural genomics]] | ||
| - | ''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 16:58:39 2008'' |
Revision as of 14:58, 21 February 2008
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Solution structure of the Helicase and RNase D C-terminal domain in Werner syndrome ATP-dependent helicase
Disease
Known diseases associated with this structure: Werner syndrome OMIM:[604611]
About this Structure
2DGZ 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 16:58:39 2008
Categories: Homo sapiens | Single protein | Abe, C. | Inoue, M. | Kigawa, T. | Muto, Y. | RSGI, RIKEN Structural Genomics/Proteomics Initiative. | Shirouzu, M. | Terada, T. | Yokoyama, S. | Hrdc domain | National project on protein structural and functional analyses | Nppsfa | Riken structural genomics/proteomics initiative | Rsgi | Structural genomics
