2osa
From Proteopedia
(Difference between revisions)
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
- | [[Category: Arrowsmith, C | + | [[Category: Arrowsmith, C H.]] |
[[Category: Bochkarev, A.]] | [[Category: Bochkarev, A.]] | ||
- | [[Category: Edwards, A | + | [[Category: Edwards, A M.]] |
- | [[Category: Hong, B | + | [[Category: Hong, B S.]] |
- | [[Category: Park, H | + | [[Category: Park, H W.]] |
- | [[Category: SGC, Structural | + | [[Category: SGC, Structural Genomics Consortium.]] |
[[Category: Shen, L.]] | [[Category: Shen, L.]] | ||
[[Category: Sundstrom, M.]] | [[Category: Sundstrom, M.]] | ||
- | [[Category: Walker, J | + | [[Category: Walker, J R.]] |
[[Category: Weigelt, J.]] | [[Category: Weigelt, J.]] | ||
[[Category: gtpase activation]] | [[Category: gtpase activation]] | ||
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[[Category: structural genomics consortium]] | [[Category: structural genomics consortium]] | ||
- | ''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 18:22:04 2008'' |
Revision as of 16:22, 21 February 2008
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The Rho-GAP domain of human N-chimaerin
Disease
Known diseases associated with this structure: Hypothyroidism, congenital, nongoitrous OMIM:[609893], Leukemia, juvenile myelomonocytic OMIM:[605370]
About this Structure
2OSA 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 18:22:04 2008
Categories: Homo sapiens | Single protein | Arrowsmith, C H. | Bochkarev, A. | Edwards, A M. | Hong, B S. | Park, H W. | SGC, Structural Genomics Consortium. | Shen, L. | Sundstrom, M. | Walker, J R. | Weigelt, J. | Gtpase activation | Rho-gap | Sgc | Structural genomics | Structural genomics consortium