2dgz: 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
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- 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
