1rg6
From Proteopedia
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(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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Revision as of 16:56, 12 November 2007
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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 Mon Nov 12 19:03:13 2007
