1rg6
From Proteopedia
(Difference between revisions)
(New page: 200px<br /> <applet load="1rg6" size="450" color="white" frame="true" align="right" spinBox="true" caption="1rg6" /> '''Solution structure of the C-terminal domain...) |
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| - | [[Image:1rg6.gif|left|200px]]<br /> | + | [[Image:1rg6.gif|left|200px]]<br /><applet load="1rg6" size="350" color="white" frame="true" align="right" spinBox="true" |
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caption="1rg6" /> | caption="1rg6" /> | ||
'''Solution structure of the C-terminal domain of p63'''<br /> | '''Solution structure of the C-terminal domain of p63'''<br /> | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1RG6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http:// | + | 1RG6 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RG6 OCA]. |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Cadot, B.]] | [[Category: Cadot, B.]] | ||
[[Category: Candi, E.]] | [[Category: Candi, E.]] | ||
| - | [[Category: Cicero, D | + | [[Category: Cicero, D O.]] |
[[Category: Desideri, A.]] | [[Category: Desideri, A.]] | ||
[[Category: Mele, S.]] | [[Category: Mele, S.]] | ||
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[[Category: p73 sam-like domain]] | [[Category: p73 sam-like domain]] | ||
| - | ''Page seeded by [http:// | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 14:50:35 2008'' |
Revision as of 12:50, 21 February 2008
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Solution structure of the C-terminal domain of p63
Disease
Known diseases associated with this structure: ADULT syndrome OMIM:[603273], Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 OMIM:[603273], Hay-Wells syndrome OMIM:[603273], Limb-mammary syndrome OMIM:[603273], Orofacial cleft 8 OMIM:[603273], Rapp-Hodgkin syndrome OMIM:[603273], Split-hand/foot malformation, type 4 OMIM:[603273]
About this Structure
1RG6 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 14:50:35 2008
