1rg6 | pdb_00001rg6
From Proteopedia
Solution structure of the C-terminal domain of p63
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| 1rg6 | |||||||||||||
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| Gene: | p63 (Homo sapiens) | ||||||||||||
| Coordinates: | save as pdb, mmCIF, xml | ||||||||||||
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 Mar 20 13:51:09 2008
